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calendar

12,161 catalysts · 3,603 8k filing · 2,283 grant · 1,765 approval · 1,146 device 510k · 1,000 device adverse event · 827 device pma

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  • 8k filing3,603
  • grant2,283
  • approval1,765
  • device 510k1,146
  • device adverse event1,000
  • device pma827
  • device recall606
  • earnings585
  • recall266
  • phase 2 completion172
  • therapy area
    • Oncology148
    • Infectious Disease46
    • Cardiology37
    • Immunology35
    • Dermatology31
    • Pulmonology22
    • Women's Health19
    • Ophthalmology16
    • Pain15

    Week of Dec 15, 2025

    50
    ›Dec 15, 2025device pma257d agoEBR Systems, Inc. — WiSE® (Wireless Stimulation of the Endocardium Technology) CRT System (PMA supplement)EBR Systems, Inc.

    Supplement type: 30-Day Notice. Product code: SEG. Advisory committee: CV. Decision: OK30

    full page →fda device pma ↗
    ›Dec 15, 2025device pma257d agoDepuy, Inc. — LCS Total Knee System (PMA supplement)

    Supplement type: 30-Day Notice. Product code: NJL. Advisory committee: OR. Decision: OK30

    full page →fda device pma ↗
    ›Dec 15, 2025device pma257d agoBoston Scientific Corp — WATCHMAN FLX™ Pro Left Atrial Appendage Closure Device with Delivery System (PMA supplement)BOSTON SCIENTIFIC CORP

    Supplement type: Normal 180 Day Track No User Fee. Product code: NGV. Advisory committee: CV. Decision: APPR

    full page →fda device pma ↗
    ›Dec 15, 2025device pma257d agoUrotronic, Inc. — Optilume™ BPH Catheter System (PMA supplement)

    Supplement type: Normal 180 Day Track No User Fee. Product code: QXB. Advisory committee: GU. Decision: APPR

    full page →fda device pma ↗
    ›Dec 15, 2025device pma257d agoBoston Scientific Corp — WATCHMAN FLX™ Pro Left Atrial Appendage Closure Device with Delivery System (PMA supplement)BOSTON SCIENTIFIC CORP

    Supplement type: Normal 180 Day Track No User Fee. Product code: NGV. Advisory committee: CV. Decision: APPR

    full page →fda device pma ↗
    ›Dec 15, 2025device pma257d agoETHICON, Inc. — ETHIZIA (PMA)

    Product code: SGV. Advisory committee: SU. Decision: APPR

    full page →fda device pma ↗
    ›Dec 15, 2025device pma257d agoVentana Medical Systems, Inc. — HER2 Dual ISH DNA Probe Cocktail (PMA supplement)MERIT MEDICAL SYSTEMS INC

    Supplement type: Normal 180 Day Track. Product code: NYQ. Advisory committee: PA. Decision: APPR

    full page →fda device pma ↗
    ›Dec 15, 2025device pma257d agoMedibeacon, Inc. — MediBeacon® Transdermal GFR Measurement System (TGFR) (PMA supplement)

    Supplement type: Normal 180 Day Track. Product code: SDK. Advisory committee: GU. Decision: APPR

    full page →fda device pma ↗
    ›Dec 15, 2025device pma257d agoMedtronic, Inc. — Aurora EV-ICD System (PMA supplement)Medtronic plc

    Supplement type: 30-Day Notice. Product code: LWS. Advisory committee: CV. Decision: OK30

    full page →fda device pma ↗
    ›Dec 15, 2025device pma257d agoScibase AB — Nevisense (PMA supplement)

    Supplement type: 30-Day Notice. Product code: ONV. Advisory committee: SU. Decision: OK30

    full page →fda device pma ↗
    ›Dec 15, 2025device pma257d agoMedtronic Cardiac Rhythm Disease Management — Cobalt MRI ICD DDPB3D4, DVPB3D4; Cobalt XT MRI ICD DDPA2D4, DVPA2D4; Crome MRI ICD DDPC3D4, DVPC3D4; Evera MRI DF-1 ICD (PMA supplement)

    Supplement type: 30-Day Notice. Product code: LWS. Advisory committee: CV. Decision: OK30

    full page →fda device pma ↗
    ›Dec 15, 2025device pma257d agoRoche Molecular Systems, Inc. — COBAS HPV TEST (PMA supplement)

    Supplement type: 30-Day Notice. Product code: MAQ. Advisory committee: MI. Decision: OK30

    full page →fda device pma ↗
    ›Dec 15, 2025device recall257d agoImmunotech A.S. device recall (Cls II)AIM ImmunoTech Inc.

    Estrone RIA, REF: DSL8700 — Reason: The affected Estrone RIA kit lots may rarely give falsely high patient results which might cause Temporary injury of Remote probability. Only in some (very rare) cases may the issue occur. — Status: Ongoing

    full page →fda device recalls ↗
    ›Dec 15, 2025device recall257d agoIntuitive Surgical, Inc. device recall (Cls II)INTUITIVE SURGICAL INC

    da Vinci SP, SP Access Port Kit, Large Incision Reference Numbers:430073 (2.7-4cm,SP1098, Box) & 430075 (2.7-7cm,SP1098,Box) — Reason: Access Port System tray may develop cracks potentially resulting in a sterility breach. — Status: Ongoing

    full page →fda device recalls ↗
    ›Dec 15, 2025device recall257d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

    Allura Xper FD10F; Model Number: 722002; — Reason: Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the implementation was not adequately documented. If it is not installed, there is a potential for coolant liquid to contact electrical components. This could lead to electrical short-circuits, which may trigger system fuses and result in system shutdown. — Status: Ongoing

    full page →fda device recalls ↗
    ›Dec 15, 2025device recall257d agoSunMed Holdings, LLC device recall (Cls I)Sagent Pharmaceuticals Inc

    Brand Name: Broselow Product Name: Broselow Pediatric Emergency Rainbow Tape Model/Catalog Number: 7700RE Software Version: Not Applicable Product Description: The Broselow Tape is a length- and weight-based reference tool specifically designed for pediatric emergency care. Component: No — Reason: Product contains potentially harmful dosing errors for Vecuronium, Flumazenil, and Ketamine. — Status: Ongoing

    full page →fda device recalls ↗
    ›Dec 15, 2025device recall257d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

    Allura Xper FD10/10; Model Number: 722027; — Reason: Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the implementation was not adequately documented. If it is not installed, there is a potential for coolant liquid to contact electrical components. This could lead to electrical short-circuits, which may trigger system fuses and result in system shutdown. — Status: Ongoing

    full page →fda device recalls ↗
    ›Dec 15, 2025device recall257d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

    Allura Xper FD20; Model Number: 722028; — Reason: Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the implementation was not adequately documented. If it is not installed, there is a potential for coolant liquid to contact electrical components. This could lead to electrical short-circuits, which may trigger system fuses and result in system shutdown. — Status: Ongoing

    full page →fda device recalls ↗
    ›Dec 15, 2025device recall257d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

    Product Name: Allura Xper FD10C; Model number: 722001; — Reason: Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the implementation was not adequately documented. If it is not installed, there is a potential for coolant liquid to contact electrical components. This could lead to electrical short-circuits, which may trigger system fuses and result in system shutdown. — Status: Ongoing

    full page →fda device recalls ↗
    ›Dec 15, 2025device recall257d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

    Allura Xper FD10; Model Number: 722003; — Reason: Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the implementation was not adequately documented. If it is not installed, there is a potential for coolant liquid to contact electrical components. This could lead to electrical short-circuits, which may trigger system fuses and result in system shutdown. — Status: Ongoing

    full page →fda device recalls ↗
    ›Dec 15, 2025device recall257d agoICU Medical, Inc. device recall (Cls II)ICU MEDICAL INC/DE

    ICU Medical Plum Duo Infusion Pump, List Numbers: 400020401 (US), 400021001 (Philippines) — Reason: Plum Solo and Duo Infusion pumps include a feature, that when selected, automatically flushes the downstream line after a piggyback therapy. The programmed flush volume is delivered from the primary line container at the piggyback therapy rate after the piggyback therapy is complete. In certain cases, as described below, the clinician may receive an Upper Hard Limit (UHL) or Lower Hard Limit (LHL) Violation message when programming a piggyback flush, which prevents the flush from being programmed. — Status: Ongoing

    full page →fda device recalls ↗
    ›Dec 15, 2025device recall257d agoICU Medical, Inc. device recall (Cls II)ICU MEDICAL INC/DE

    ICU Medical Plum Solo Precision IV Pump, List Numbers: 400010401 (US), 400011001 (Philippines) — Reason: Plum Solo and Duo Infusion pumps include a feature, that when selected, automatically flushes the downstream line after a piggyback therapy. The programmed flush volume is delivered from the primary line container at the piggyback therapy rate after the piggyback therapy is complete. In certain cases, as described below, the clinician may receive an Upper Hard Limit (UHL) or Lower Hard Limit (LHL) Violation message when programming a piggyback flush, which prevents the flush from being programmed. — Status: Ongoing

    full page →fda device recalls ↗
    ›Dec 15, 2025device recall257d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

    Allura Xper FD10/10; Model Number: 722011; — Reason: Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the implementation was not adequately documented. If it is not installed, there is a potential for coolant liquid to contact electrical components. This could lead to electrical short-circuits, which may trigger system fuses and result in system shutdown. — Status: Ongoing

    full page →fda device recalls ↗
    ›Dec 15, 2025device recall257d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

    Allura Xper FD20/20; Model Number: 722038; — Reason: Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the implementation was not adequately documented. If it is not installed, there is a potential for coolant liquid to contact electrical components. This could lead to electrical short-circuits, which may trigger system fuses and result in system shutdown. — Status: Ongoing

    full page →fda device recalls ↗
    ›Dec 15, 2025device recall257d agoLEASEIR TECHNOLOGIES SLU device recall (Cls II)

    Brand Name: LEASEIR Product Name: LEASEIR MHR XCELL Model/Catalog Number: MHR 110-b Software Version: 1.5.0.0 Product Description: The Leaseir MHR Xcell is a surgical laser instrument for use in general and plastic surgery and dermatology, intended for hair removal and treatment of pseudo folliculitis barbae on all skin types (Fitzpatrick I-VI). The process implies the generation of intense light pulses at specific wavelengths. The specific nature of the energies and pulse durations cause the desired effect (in the hair follicles and oxyhemoglobin in the blood) heating them sufficiently and destroying them without unnecessary damage to surrounding tissue. This is achieved by controlled emission of laser radiation to the target tissue. The system consists of a main console and two interchangeable applicators that delivers pulsed light in the range of 800-820nm with a peak in the 810nm in different spot sizes. Two of the applicators emitting radiation at 810 nm wavelength for two areas 13.5¿15 mm¿ and 14.5¿25.5 mm¿. Two different operation modes are available: static mode and dynamic mode, which are differentiated basically by the frequency range defined for each mode (1-4 Hz for static and 10 Hz for dynamic). The principle of operation consists in the photons travel along the axis and reflected again back into the crystal, continuing the chain reaction, while photons travelling in different directions leave the crystal. In one of the two mirrors, a tiny hole allows a small amount of light to leak out and the resulting beam is focused with lenses and is emitted from the laser. The total energy emitted by the Leaseir MHR Xcell is produced by an array of diodes. The laser emission is activated by the hand piece trigger, deliver a continuous pulse pattern while the button is pressed. Component: NO — Reason: The console label for affected devices is missing the "DANGER" symbol. — Status: Ongoing

    ›Dec 15, 2025device recall257d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

    Allura Xper FD10/10; Model Number: 722005; — Reason: Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the implementation was not adequately documented. If it is not installed, there is a potential for coolant liquid to contact electrical components. This could lead to electrical short-circuits, which may trigger system fuses and result in system shutdown. — Status: Ongoing

    full page →fda device recalls ↗
    ›Dec 15, 2025device recall257d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

    Allura Xper FD20; Model Number: 722012; — Reason: Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the implementation was not adequately documented. If it is not installed, there is a potential for coolant liquid to contact electrical components. This could lead to electrical short-circuits, which may trigger system fuses and result in system shutdown. — Status: Ongoing

    full page →fda device recalls ↗
    ›Dec 15, 2025device recall257d agoDiagnostica Stago, Inc. device recall (Cls II)

    Asserachrom HPIA. Model/Catalog Number: 00615. The Asserachrom HPIA kit is intended for the qualitative detection in plasma or serum of the anti-heparin-platelet factor 4 (PF4) antibodies generated during the type II heparin-induced thrombocytopenia (HIT type II) by ELISA. — Reason: Potential for defect for Asserachrom HPIA lot 271288, which can affect every well in the impacted strip and produce negative results. — Status: Ongoing

    full page →fda device recalls ↗
    ›Dec 15, 2025device recall257d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

    Allura Xper FD20/10; Model Number: 722029; — Reason: Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the implementation was not adequately documented. If it is not installed, there is a potential for coolant liquid to contact electrical components. This could lead to electrical short-circuits, which may trigger system fuses and result in system shutdown. — Status: Ongoing

    full page →fda device recalls ↗
    ›Dec 15, 2025device recall257d agoICU Medical, Inc. device recall (Cls II)ICU MEDICAL INC/DE

    ICU Medical Plum Duo Precision IV Pump, List Numbers: 400020403 (US), 400021003 (Philippines) — Reason: Plum Solo and Duo Infusion pumps include a feature, that when selected, automatically flushes the downstream line after a piggyback therapy. The programmed flush volume is delivered from the primary line container at the piggyback therapy rate after the piggyback therapy is complete. In certain cases, as described below, the clinician may receive an Upper Hard Limit (UHL) or Lower Hard Limit (LHL) Violation message when programming a piggyback flush, which prevents the flush from being programmed. — Status: Ongoing

    full page →fda device recalls ↗
    ›Dec 15, 2025device recall257d agoSunMed Holdings, LLC device recall (Cls I)Sagent Pharmaceuticals Inc

    Brand Name: Broselow Product Name: Broselow Domestic Complete ALS Organizer Model/Catalog Number: 7730ALS Software Version: Not Applicable Product Description: The Broselow Tape is a length- and weight-based reference tool specifically designed for pediatric emergency care. Component: No — Reason: Product contains potentially harmful dosing errors for Vecuronium, Flumazenil, and Ketamine. — Status: Ongoing

    full page →fda device recalls ↗
    ›Dec 15, 2025device recall257d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

    Allura Xper FD10; Model Number: 722010; — Reason: Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the implementation was not adequately documented. If it is not installed, there is a potential for coolant liquid to contact electrical components. This could lead to electrical short-circuits, which may trigger system fuses and result in system shutdown. — Status: Ongoing

    full page →fda device recalls ↗
    ›Dec 15, 2025device recall257d agoSysmex America, Inc. device recall (Cls II)

    TS-10/TS-10H Tube Sorter, automatic sorting system for sorting barcoded sample tubes, Catalog Number BN168792, running software versions 00-17 — Reason: Under specific conditions, the lift's electromagnetic holding force may disengage unexpectedly, allowing unintended downward movement of the lift. — Status: Ongoing

    full page →fda device recalls ↗
    ›Dec 15, 2025device recall257d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

    Allura Xper FD20 Biplane; Model Number: 722008; — Reason: Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the implementation was not adequately documented. If it is not installed, there is a potential for coolant liquid to contact electrical components. This could lead to electrical short-circuits, which may trigger system fuses and result in system shutdown. — Status: Ongoing

    full page →fda device recalls ↗
    ›Dec 15, 2025device recall257d agoSunMed Holdings, LLC device recall (Cls I)Sagent Pharmaceuticals Inc

    Brand Name: Broselow Product Name: BROSELOW" FILLED BROSELOW ORGANIZER Model/Catalog Number: 7730IALS Software Version: Not Applicable Product Description: The Broselow Tape is a length- and weight-based reference tool specifically designed for pediatric emergency care. Component: no — Reason: Product contains potentially harmful dosing errors for Vecuronium, Flumazenil, and Ketamine. — Status: Ongoing

    full page →fda device recalls ↗
    ›Dec 15, 2025device recall257d agoICU Medical, Inc. device recall (Cls II)ICU MEDICAL INC/DE

    Plum Duo Infusion System, List Number 40002-04-01 — Reason: ICU Medical received one lot of defective primary speakers from our supplier that may fail to produce an audible sound. If the primary speaker in your Plum Duo Infusion Pump fails, the pump may not produce audible alarms, alerts, or provide audible feedback for touchscreen inputs. — Status: Ongoing

    full page →fda device recalls ↗
    ›Dec 15, 2025device recall257d agoSunMed Holdings, LLC device recall (Cls I)Sagent Pharmaceuticals Inc

    Brand Name: Broselow Product Name: Broselow Pediatric Emergency Rainbow Tape Model/Catalog Number: 7700REA Software Version: Not Applicable Product Description: The Broselow Tape is a length- and weight-based reference tool specifically designed for pediatric emergency care. Component: No — Reason: Product contains potentially harmful dosing errors for Vecuronium, Flumazenil, and Ketamine. — Status: Ongoing

    full page →fda device recalls ↗
    ›Dec 15, 2025device recall257d agoHologic, Inc device recall (Cls II)

    Brevera Breast Biopsy System Disposable 9 Gauge Needle. Biopsy Instrument. — Reason: Presence of particulates in affected devices that can be deposited into breast tissue during use. — Status: Ongoing

    full page →fda device recalls ↗
    ›Dec 15, 2025device recall257d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

    Allura Xper FD20 OR Table; Model Number: 722023; — Reason: Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the implementation was not adequately documented. If it is not installed, there is a potential for coolant liquid to contact electrical components. This could lead to electrical short-circuits, which may trigger system fuses and result in system shutdown. — Status: Ongoing

    full page →fda device recalls ↗
    ›Dec 15, 2025device recall257d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

    Allura Xper FD20 Biplane; Model Number: 722013; — Reason: Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the implementation was not adequately documented. If it is not installed, there is a potential for coolant liquid to contact electrical components. This could lead to electrical short-circuits, which may trigger system fuses and result in system shutdown. — Status: Ongoing

    full page →fda device recalls ↗
    ›Dec 15, 2025device recall257d agoWilson-Cook Medical Inc. device recall (Cls II)

    Product Name: Nasal Jejunal Feeding Tube REF: NJFT-10 — Reason: Nasal feeding tube packaged without the nasal transfer tube component. — Status: Ongoing

    full page →fda device recalls ↗
    ›Dec 15, 2025device recall257d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

    Allura Xper FD10; Model Number: 722026; — Reason: Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the implementation was not adequately documented. If it is not installed, there is a potential for coolant liquid to contact electrical components. This could lead to electrical short-circuits, which may trigger system fuses and result in system shutdown. — Status: Ongoing

    full page →fda device recalls ↗
    ›Dec 15, 2025device recall257d agoPHILIPS MEDICAL SYSTEMS NEDERLAND B.V. device recall (Cls II)

    Allura Xper FD20; Model Number: 722006; — Reason: Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the implementation was not adequately documented. If it is not installed, there is a potential for coolant liquid to contact electrical components. This could lead to electrical short-circuits, which may trigger system fuses and result in system shutdown. — Status: Ongoing

    full page →fda device recalls ↗
    ›Dec 15, 2025grant257d agoJACKSON LABORATORY — Genetic dissection of microglia functions in complement-mediated synapse loss...

    AG grant. $716,579. PI: Erik Bradley Bloss

    full page →nih reporter ↗
    ›Dec 15, 2025grant257d agoUNIVERSITY OF VIRGINIA — Model-Based Syllabic Prediction in the Avian Auditory PalliumUniversity of Virginia

    DC grant. $41,394. PI: Bao Le

    full page →nih reporter ↗
    ›Dec 15, 2025grant257d agoRUTGERS BIOMEDICAL AND HEALTH SCIENCES — The Role of APP-metabolites on Extracellular Vesicle Cargo and Function

    AG grant. $639,838. PI: MARC D TAMBINI

    full page →nih reporter ↗
    ›Dec 15, 2025grant257d agoCLEVELAND CLINIC LERNER COM-CWRU — Endothelial TLR2/4 signaling in sex dimorphism of pathological angiogenesis a...

    AG grant. $659,309. PI: Tatiana V Byzova

    full page →nih reporter ↗
    ›Dec 15, 2025grant257d agoUNIVERSITY OF MISSOURI-COLUMBIA — Targeting LARP6 in aging-associated heart failure

    AG grant. $429,394. PI: Shawn Brady Bender

    full page →nih reporter ↗
    ›Dec 16, 2025approval256d agoTIZANIDINE HYDROCHLORIDE — FDA approvalTIZANIDINE HYDROCHLORIDE

    Sponsor: APOTEX INC. Form: CAPSULE. Route: ORAL

    full page →TIZANIDINE HYDROCHLORIDE →fda approvals ↗
    ›Dec 16, 2025approval256d agoHYMPAVZI (MARSTACIMAB-HNCQ) — FDA approvalmarstacimab

    Sponsor: PFIZER INC. Form: INJECTABLE. Route: SUBCUTANEOUS

    full page →marstacimab →fda approvals ↗
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    full page →fda device recalls ↗
    $EBRCZ0.2780+48.56%
    $ISRG372.60+1.51%
    $ICUI175.100.00%
    $MDT91.23+1.40%
    $MMSI90.49+1.06%
    $ICUI175.100.00%
    $AIM
    $BSX47.53-1.33%
    $BSX47.53-1.33%
    $ICUI175.100.00%
    $ICUI175.100.00%
    $PFE28.03-0.96%