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18,881 catalysts · 4,728 grant · 3,431 8k filing · 2,667 approval · 2,309 device 510k · 1,852 device recall · 1,612 device pma

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  • grant4,728
  • 8k filing3,431
  • approval2,667
  • device 510k2,309
  • device recall1,852
  • device pma1,612
device adverse event
1,000
  • recall617
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    • Oncology148
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    Week of Sep 15, 2025

    50
    ›Sep 17, 2025grant337d agoRAIZ DIAGNOSTICS, INC. — Scaling Lymphoma Diagnosis: A Cost-Effective Gene Expression Assay for Broad ...

    CA grant. $1,770,000. PI: Edward Briercheck

    full page →nih reporter ↗
    ›Sep 17, 2025grant337d agoOHIO STATE UNIVERSITY — Clinical and Translational Data Science Training Program

    TR grant. $252,545. PI: Kellie J. Archer

    full page →nih reporter ↗
    ›Sep 17, 2025grant337d agoUNIVERSITY OF COLORADO DENVER — Advancing Cancer Screening and Prevention Trials at the University of Colorad...University of Colorado Denver

    CA grant. $547,080. PI: Marie E. Wood

    full page →nih reporter ↗
    ›Sep 17, 2025grant337d agoUNIVERSITY OF COLORADO DENVER — Integrating genomic architecture and tuberculosis (TB) immunity in AfricaUniversity of Colorado Denver

    AI grant. $802,499. PI: Paul John Norman

    full page →nih reporter ↗
    ›Sep 17, 2025grant337d agoEMORY UNIVERSITY — The molecular mechanisms underlying context-specific Runx factor functions in...Emory University

    HL grant. $248,999. PI: Boyoung Shin

    full page →nih reporter ↗
    ›Sep 17, 2025grant337d agoUNIVERSITY OF CALIFORNIA, SAN FRANCISCO — Rapid Research for Diagnostics Development in TB Network: Episode 2 (R2D2 TB ...University of California San Francisco

    AI grant. $455,914. PI: Adithya Cattamanchi

    full page →nih reporter ↗
    ›Sep 17, 2025grant337d agoUNIV OF MASSACHUSETTS MED SCH WORCESTER — An investigation of sex differences in excessive alcohol use in young adultho...

    AA grant. $167,500. PI: Kathryn Sabella

    full page →nih reporter ↗
    ›Sep 17, 2025grant337d agoUNIVERSITY OF VIRGINIA — A Phase II Trial to Prevent Linear Growth Stunting and Malnutrition in Impove...University of Virginia

    HD grant. $144,767. PI: Jeffrey Ryan Donowitz

    full page →nih reporter ↗
    ›Sep 17, 2025grant337d agoPONS INCORPORATED — Development of an automated image enhancement system to improve point-of-care...

    MD grant. $337,355. PI: Ilker Hacihaliloglu

    full page →nih reporter ↗
    ›Sep 17, 2025grant337d agoSOJOURN MEDTECH LLC — Patient-Centered Self-Cannulation Training Simulator to Promote Self-Care and...Piramal Critical Care Inc

    MD grant. $349,859. PI: ABHIJIT V KSHIRSAGAR

    full page →nih reporter ↗
    ›Sep 18, 2025device 510k336d agoAxial Medical Printing Limited — Axial3D Insight (510k cleared)

    Product code: QIH. Advisory committee: Radiology. Type: Traditional

    full page →fda device 510k ↗
    ›Sep 18, 2025device 510k336d agoMedela AG — Magic InBra (510k cleared)

    Product code: HGX. Advisory committee: Obstetrics/Gynecology. Type: Traditional

    full page →fda device 510k ↗
    ›Sep 18, 2025device 510k336d agoShenB Co., Ltd. — Sunny Plus (Sunny) (510k cleared)

    Product code: NFO. Advisory committee: Neurology. Type: Traditional

    full page →fda device 510k ↗
    ›Sep 18, 2025device 510k336d agoOlympus Medical Systems Corporation — ULTRASONIC PROBE UM-3R (UM-3R); ULTRASONIC PROBE UM-G20-29R (UM-G20-29R) (510k cleared)

    Product code: ITX. Advisory committee: Radiology. Type: Traditional

    full page →fda device 510k ↗
    ›Sep 18, 2025device 510k336d agoMobarn Medical Devices, LLC — Mobarn 80:20 Lumbar Interbody Fusion System (Posterior Lumbar Interbody Fusion Cage (PLIF)); Mobarn 80:20 Lumbar Interbody Fusion System (Transforaminal Lumbar Interbody Fusion Cage (TLIF)); Mobarn 80:20 Lumbar Interbody Fusion System (Direct Lateral Lumbar Interbody Fusion Cage (DLIF)); Mobarn 80:20 Lumbar Interbody Fusion System (Anterior Lumbar Interbody Fusion Cage (ALIF)) (510k cleared)

    Product code: MAX. Advisory committee: Orthopedic. Type: Traditional

    full page →fda device 510k ↗
    ›Sep 18, 2025device 510k336d agoNormaTec Industries, LP — Normatec Elite Hip (510k cleared)

    Product code: IRP. Advisory committee: Physical Medicine. Type: Traditional

    full page →fda device 510k ↗
    ›Sep 18, 2025device 510k336d agoSuperpi Robot Co., Ltd. — Electric Wheelchair (Model P2) (510k cleared)

    Product code: ITI. Advisory committee: Physical Medicine. Type: Traditional

    full page →fda device 510k ↗
    ›Sep 18, 2025device 510k336d agoPerimetrics, Inc. — InnerView System (510k cleared)

    Product code: EKX. Advisory committee: Dental. Type: Traditional

    full page →fda device 510k ↗
    ›Sep 18, 2025device pma336d agoMedtronic Neuromodulation — Medtronic Altaviva System (PMA)

    Product code: QPT. Advisory committee: GU. Decision: APPR

    full page →fda device pma ↗
    ›Sep 18, 2025device pma336d agoMedtronic, Inc. — Activa® Deep Brain Stimulation Therapy System, Percept™ PC BrainSense™ (DBS Neurostimulator Implantable B35200); (DBS Ne (PMA supplement)Medtronic plc

    Supplement type: 30-Day Notice. Product code: MHY. Advisory committee: NE. Decision: OK30

    full page →fda device pma ↗
    ›Sep 18, 2025device pma336d agoMedtronic Neuromodulation — InterStim® Therapy System, Verify® Evaluation System (SNS Bowel Neurostimulator 97800); (SNS Bowel Neurostimulators Impl (PMA supplement)

    Supplement type: 30-Day Notice. Product code: QON. Advisory committee: GU. Decision: OK30

    full page →fda device pma ↗
    ›Sep 18, 2025device pma336d agoMicroVention, Inc. — FRED X System (PMA supplement)MICROVISION, INC.

    Supplement type: Real-Time Process. Product code: OUT. Advisory committee: NE. Decision: APPR

    full page →fda device pma ↗
    ›Sep 18, 2025device pma336d agoSiemens Healthcare Diagnostics Products, Ltd. — IMMULITE 2000 Hepatitis B Surface Antigen (HBsAg), IMMULITE 2000 Hepatitis B Surface Antigen (HBsAg) Confirmatory Kit (PMA supplement)

    Supplement type: 135 Review Track For 30-Day Notice. Product code: LOM. Advisory committee: MI. Decision: APPR

    full page →fda device pma ↗
    ›Sep 18, 2025device pma336d agoAlcon Laboratories, Inc. — AcrySof® Posterior Chamber Intraocular Lens and Delivery Systems (PMA supplement)Alcon Laboratories Inc

    Supplement type: 30-Day Notice. Product code: HQL. Advisory committee: OP. Decision: OK30

    full page →fda device pma ↗
    ›Sep 18, 2025device pma336d agoEndologix, LLC — DETOUR System (PMA supplement)

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

    full page →fda device pma ↗
    ›Sep 18, 2025device pma336d agoABBOTT MEDICAL — Amplatzer™ Amulet™ Left Atrial Appendage Occluder (PMA supplement)

    Supplement type: Real-Time Process. Product code: NGV. Advisory committee: CV. Decision: APPR

    full page →fda device pma ↗
    ›Sep 18, 2025device pma336d agoTeoxane S.A. — RHA® Dynamic Volume, RHA®4 (PMA supplement)

    Supplement type: Panel Track. Product code: LMH. Advisory committee: SU. Decision: APPR

    full page →fda device pma ↗
    ›Sep 18, 2025device pma336d agoCook Medical Incorporated — ZENITH ALPHA THORACIC ENDOVASCULAR GRAFT (PMA supplement)

    Supplement type: Real-Time Process. Product code: MIH. Advisory committee: CV. Decision: APPR

    full page →fda device pma ↗
    ›Sep 18, 2025device pma336d agoMedtronic Neuromodulation — InterStim® Therapy System, Verify® Evaluation System (SNS Urinary Neurostimulator 97800); (SNS Urinary Neurostimulator I (PMA supplement)

    Supplement type: 30-Day Notice. Product code: EZW. Advisory committee: GU. Decision: OK30

    full page →fda device pma ↗
    ›Sep 18, 2025device pma336d agoAlcon Laboratories, LLC — Clareon® Aspheric Hydrophobic Acrylic Intraocular Lens (IOL), Clareon® Toric Aspheric Hydrophobic Acrylic Intraocular Le (PMA supplement)Alcon Laboratories Inc

    Supplement type: 30-Day Notice. Product code: HQL. Advisory committee: OP. Decision: OK30

    full page →fda device pma ↗
    ›Sep 18, 2025device pma336d agoAlcon Research, Ltd. — AcrySof® IQ ReSTOR® Posterior Chamber Intraocular Lenses (PMA supplement)Rubicon Research Ltd

    Supplement type: 30-Day Notice. Product code: MFK. Advisory committee: OP. Decision: OK30

    full page →fda device pma ↗
    ›Sep 18, 2025device pma336d agoMedtronic, Inc. — SynchroMed® Infusion System, Ascenda® Intrathecal Catheters (Drug Delivery Infusion Pump 8667); (Drug Delivery Infusion (PMA supplement)Medtronic plc

    Supplement type: 30-Day Notice. Product code: LKK. Advisory committee: HO. Decision: OK30

    full page →fda device pma ↗
    ›Sep 18, 2025device pma336d agoSiemens Healthcare Diagnostics Products, Ltd. — IMMULITE 2000 Hepatitis B Surface Antigen (HBsAg), IMMULITE 2000 Hepatitis B Surface Antigen (HBsAg) Confirmatory Kit (PMA supplement)

    Supplement type: 135 Review Track For 30-Day Notice. Product code: LOM. Advisory committee: MI. Decision: APPR

    full page →fda device pma ↗
    ›Sep 18, 2025device pma336d agoMedtronic Neuromodulation — Master Restore, Itrel®, Synergy®, Intellis™ and Vanta™ Spinal Cord Stimulation Systems and Pisces™, Specify®, and Vectri (PMA supplement)

    Supplement type: 30-Day Notice. Product code: LGW. Advisory committee: NE. Decision: OK30

    full page →fda device pma ↗
    ›Sep 18, 2025device pma336d agoSiemens Healthcare Diagnostics Products, Ltd. — IMMULITE 2000 Total Antibodies to Hepatitis B Surface Antigen (Anti-HBs) (PMA supplement)

    Supplement type: 135 Review Track For 30-Day Notice. Product code: LOM. Advisory committee: MI. Decision: APPR

    full page →fda device pma ↗
    ›Sep 18, 2025device recall336d agoCardinal Health 200, LLC device recall (Cls II)CARDINAL HEALTH INC

    Salem Sump PVC Tubes: Product Code/Product Name: 8888265108 Salem Sump Silicone Dual Lumen Stomach Tube, Radiopaque Line, 10 Fr/Ch (3.3 mm), 36 (91 cm) 8888265116 Salem Sump Silicone Dual Lumen Stomach Tube, Radiopaque Line, 12 Fr/Ch (4.0 mm), 48 (122 cm) 8888265124 Salem Sump Silicone Dual Lumen Stomach Tube, Radiopaque Line, 14 Fr/Ch (4.7 mm), 48 (122 cm) 8888265132 Salem Sump Silicone Dual Lumen Stomach Tube, Radiopaque Line, 16 Fr/Ch (5.3 mm), 48 (122 cm) 8888265140 Salem Sump Silicone Dual Lumen Stomach Tube, Radiopaque Line, 18 Fr/Ch (6.0 mm), 48 (122 cm) 8888266213 Salem Sump TM Silicone Dual Lumen Stomach Tube, Anti-Reflux Valve and Radiopaque Line, 10 Fr/Ch (3.3 mm) x 36 (91 cm) 8888266221 Salem Sump TM Silicone Dual Lumen Stomach Tube, Anti-Reflux Valve and Radiopaque Line, 12 Fr/Ch (4.0 mm) x 48 (122 cm) 8888266247 Salem Sump TM Silicone Dual Lumen Stomach Tube, Anti-Reflux Valve and Radiopaque Line, 14 Fr/Ch (4.7 mm) x 48 (122 cm) 8888266262 Salem Sump TM Silicone Dual Lumen Stomach Tube, Anti-Reflux Valve and Radiopaque Line, 16 Fr/Ch (5.3 mm) x 48 (122 cm) 8888266288 Salem Sump TM Silicone Dual Lumen Stomach Tube, Anti-Reflux Valve and Radiopaque Line, 18 Fr/Ch (6.0 mm) x 48 (122 cm) — Reason: Firm has received complaints regarding Anti-Reflux Valve (ARV) breakage due to excessive force during use. Firm is providing additional guidance for use. Expansion of RES 95214. — Status: Ongoing

    full page →fda device recalls ↗
    ›Sep 18, 2025device recall336d agoGE Medical Systems, LLC device recall (Cls II)

    LOGIQ P10 R4.5 HD ultrasound system with system software version R4.5.7., Model Number 5877535 — Reason: The Ultrasound-Guided Attenuation Parameter (UGAP) measurement data may display inaccurate values representing liver steatosis. This could potentially lead to inappropriate clinical decisions impacting overall care. — Status: Ongoing

    full page →fda device recalls ↗
    ›Sep 18, 2025device recall336d agoB BRAUN MEDICAL INC device recall (Cls II)B. Braun Medical Inc

    PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga. x 3-1/2 in. (8.9 cm) Tuohy Epidural Needle - Winged and 19 Ga. Closed tip PERIFIX FX Springwound Epidural Catheter. Product Code: CE17TKFC. Product Description: CE17TKFC EPIDURAL TRAY W/ 17GA TUOHY. — Reason: Potential for the lid of the catheter connector to be in the incorrect position. — Status: Ongoing

    full page →fda device recalls ↗
    ›Sep 18, 2025device recall336d agoCardinal Health 200, LLC device recall (Cls II)CARDINAL HEALTH INC

    Salem Sump PVC Tubes: Product Code/Product Name: 264929 Salem Sump" Stomach Tube, Dual Lumen, 12 Fr/Ch (4.0 mm) 264945 Salem Sump" Stomach Tube, Dual Lumen, 14 Fr/Ch (4.7 mm) 264960 Salem Sump" Stomach Tube, Dual Lumen, 16 Fr/Ch (5.3 mm) 264986 Salem Sump" Stomach Tube, Dual Lumen, 18 Fr/Ch (6.0 mm) 5558264957 Salem Sump" COILED TUBE 16Fr/Ch (5.3 mm) 5558264965 Salem Sump" TUBE 16 Fr/Ch (5.3 mm) 5558264973 Salem Sump" COILED TUBE 18Fr/Ch (6.0 mm) 5558264981 Salem Sump" TUBE 18 Fr/Ch 18Fr/Ch (6.0 mm) 8888264911 Salem Sump" Dual Lumen Stomach Tube, 10 Fr/Ch (3.3 mm), 36" (91 cm) 8888268060 Salem Sump" Dual Lumen Stomach Tube 6 Fr/Ch (2.0 mm), 24" (61 cm) 8888268086 Salem Sump" Dual Lumen Stomach Tube, 8 Fr/Ch (2.7 mm), 24" (61 cm) — Reason: Firm has received complaints regarding Anti-Reflux Valve (ARV) breakage due to excessive force during use. Firm is providing additional guidance for use. Expansion of RES 95214. — Status: Ongoing

    full page →fda device recalls ↗
    ›Sep 18, 2025device recall336d agoCardinal Health 200, LLC device recall (Cls II)CARDINAL HEALTH INC

    Salem Sump PVC Tubes: Product Code/Product Name: 1180264408 Salem Sump" PVC Gastroduodenal Tube, 10 Fr/Ch (3.3 mm) x 90 cm 1180264416 Salem Sump" PVC Gastroduodenal Tube, 12 Fr/Ch (4.0 mm) x 114 cm 1180264424 Salem Sump" PVC Gastroduodenal Tube, 14 Fr/Ch (4.7 mm) x 114 cm 1180264432 Salem Sump" PVC Gastroduodenal Tube, 16 Fr/Ch (5.3 mm) x 114 cm 1180264440 Salem Sump" PVC Gastroduodenal Tube, 18 Fr/Ch (6.0 mm) x 114 cm 1180264457 Salem Sump" PVC Gastroduodenal Tube, 20 Fr/Ch (6.7 mm) x 114 cm 1180264523 Salem Sump" Polyurethane Gastroduodenal Tube, 14 Fr/Ch (4.7 mm) x 114 cm 1180264531 Salem Sump" Polyurethane Gastroduodenal Tube, 16 Fr/Ch (5.3 mm) x 114 cm 1180264549 Salem Sump" Polyurethane Gastroduodenal Tube, 18 Fr/Ch (6.0 mm) x 114 cm 1180264556 Salem Sump" Polyurethane Gastroduodenal Tube, 20 Fr/Ch (6.7 mm) x 114 cm 1180264895 Salem Sump PVC Gastroduodenal Tube, 20 Fr/Ch (3.3mm), 108 cm 8888264804 Salem Sump PVC Gastroduodenal Tube, 10Fr/Ch (3.3 mm) x 85 cm 8888264820 Salem Sump PVC Gastroduodenal Tube, 12 Fr/Ch (4.0 mm) x 108 cm 8888264846 Salem Sump PVC Gastroduodenal Tube, 14 Fr/Ch (4.7mm), 108 cm 8888264861 Salem Sump PVC Gastroduodenal Tube, 16 Fr/Ch (5.3mm), 108 cm 8888264887 Salem Sump PVC Gastroduodenal Tube, 18 Fr/Ch (6.0mm), 108 cm SKUs not distributed in US — Reason: Firm has received complaints regarding Anti-Reflux Valve (ARV) breakage due to excessive force during use. Firm is providing additional guidance for use. Expansion of RES 95214. — Status: Ongoing

    full page →
    ›Sep 18, 2025device recall336d agoB BRAUN MEDICAL INC device recall (Cls II)B. Braun Medical Inc

    Combined Spinal and Epidural Anesthesia Tray 2, PERIFIX 17 Ga. x 3-1/2 in. (8.9 cm) Tuohy Epidural Needle, PENCAN 27 Ga. x 5 in. (12.7 cm) Spinal Needle, and 19 Ga. Closed Tip PERIFIX FX Springwound Epidural Catheter. Product Code: SESK. Product Description: SESK COMBINED SPINAL AND EPIDURAL TRAY 2. — Reason: Potential for the lid of the catheter connector to be in the incorrect position. — Status: Ongoing

    full page →fda device recalls ↗
    ›Sep 18, 2025device recall336d agoB BRAUN MEDICAL INC device recall (Cls II)B. Braun Medical Inc

    Combined Spinal and Epidural Anesthesia Tray, PERIFIX 17 Ga. x 3-1/2 in. (8.9 cm) Tuohy Epidural Needle, PENCAN 27 Ga. x 5 in. (12.7 cm) Spinal Needle and 19 Ga. Open Tip PERIFIX FX Springwound Epidural Catheter. Product Code: NES1727KFX. Product Description: NES1727KFX W /17GA TUOHY 19GA SPRW OT. — Reason: Potential for the lid of the catheter connector to be in the incorrect position. — Status: Ongoing

    full page →fda device recalls ↗
    ›Sep 18, 2025device recall336d agoB BRAUN MEDICAL INC device recall (Cls II)B. Braun Medical Inc

    PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga. x 3-1/2 in. (8.9cm) Tuohy Epidural Needle - Winged and 19 Ga. Closed tip PERIFIX FX Springwound Epidural Catheter. Product Code: CE17TKFCPS. Product Description: CE17TKFCPS EPIDURAL FULL TRAY. — Reason: Potential for the lid of the catheter connector to be in the incorrect position. — Status: Ongoing

    full page →fda device recalls ↗
    ›Sep 18, 2025device recall336d agoB BRAUN MEDICAL INC device recall (Cls II)B. Braun Medical Inc

    ESPOCAN Combined Spinal and Epidural Anesthesia Tray, ESPOCAN 17 Ga. x 3-1/2 in. (8.9 cm) Tuohy Epidural Needle, PENCAN 25 Ga. x 5 in. (12.7 cm) Spinal Needle with Marking and Centering Sleeve, and 19 Ga. Closed Tip PERIFIX FX Springwound Epidural Catheter. Product Code: ES1725KFX. Product Description: ES1725KFX ESPOCAN SPINAL/EPID. TRAY. — Reason: Potential for the lid of the catheter connector to be in the incorrect position. — Status: Ongoing

    full page →fda device recalls ↗
    ›Sep 18, 2025device recall336d agoCardinal Health 200, LLC device recall (Cls II)CARDINAL HEALTH INC

    Salem Sump PVC Tubes: Product Code/Product Name: 266197 Salem Sump" Anti-Reflux Valve CE Marked 8888266197 Salem Sump" Anti-Reflux Valve — Reason: Firm has received complaints regarding Anti-Reflux Valve (ARV) breakage due to excessive force during use. Firm is providing additional guidance for use. Expansion of RES 95214. — Status: Ongoing

    full page →fda device recalls ↗
    ›Sep 18, 2025device recall336d agoCook Medical Incorporated device recall (Cls I)

    Zenith Alpha 2 Thoracic Endovascular Graft, Catalog Prefix ZTA2- Reference Part Numbers ZTA2-P-40-117-W ZTA2-P-40-167 ZTA2-P-40-167-W ZTA2-P-40-217-W ZTA2-P-42-121 ZTA2-P-42-121-W ZTA2-P-42-173 ZTA2-P-42-173-W ZTA2-P-42-225 ZTA2-P-42-225-W ZTA2-P-44-125 ZTA2-P-44-125-W ZTA2-P-44-179 ZTA2-P-44-179-W ZTA2-P-44-233 ZTA2-P-44-233-W ZTA2-P-46-125 ZTA2-P-46-125-W ZTA2-P-46-179 ZTA2-P-46-179-W ZTA2-P-46-233-W ZTA2-PT-40-36-167 ZTA2-PT-40-36-167-W ZTA2-PT-40-36-217 ZTA2-PT-40-36-217-W ZTA2-PT-42-38-173 ZTA2-PT-42-38-173-W ZTA2-PT-42-38-225 ZTA2-PT-42-38-225-W ZTA2-PT-44-40-179 ZTA2-PT-44-40-179-W ZTA2-PT-44-40-233-W ZTA2-PT-46-42-179 ZTA2-PT-46-42-179-W ZTA2-PT-46-42-233 ZTA2-PT-46-42-233-W ZTA2-P-46-233 ZTA2-PT-44-40-233 ZTA2-P-40-217 ZTA2-P-40-117 ZTA2-P-40-167-DEMO ZTA2-P-44-152-W ZTA2-P-40-142 ZTA2-P-44-152 ZTA2-P-40-142-W — Reason: Affected devices may contain PTFE coating scrapings. Scrapings could be released during device deployment, potentially causing intravascular embolization. — Status: Ongoing

    full page →fda device recalls ↗
    ›Sep 18, 2025device recall336d agoB BRAUN MEDICAL INC device recall (Cls II)B. Braun Medical Inc

    PERIFIX FX Continuous Epidural Anesthesia Tray with PERIFIX 17 Ga. x 3-1/2 in. (9cm) Tuohy Epidural Needle - Winged and PERIFIX FX Springwound Catheter - 19 Ga. Closed Tip. Product Code: CE17TBFC. Product description: CE17TBFC EPIDURAL BASIC TRAY 17G TOUHY. — Reason: Potential for the lid of the catheter connector to be in the incorrect position. — Status: Ongoing

    full page →fda device recalls ↗
    ›Sep 18, 2025device recall336d agoAbbott Laboratories device recall (Cls II)ABBOTT LABORATORIES

    Brand Name: Alinity hq Analyzer Product Name: Alinity hq Analyzer Model/Catalog Number: 09P68-01 Software Version: 5.0 to 5.10.1 for OUS, 5.7 and 5.10.1 in the US Product Description: Alinity hq Analyzer Component: No — Reason: Software issue for hq analyzer results in system not visibly applying appropriate flagging to results when saturation is present which may result in incorrect results. — Status: Ongoing

    full page →fda device recalls ↗
    ›Sep 18, 2025device recall336d agoFisher & Paykel Healthcare, Ltd. device recall (Cls II)

    Airvo 2, REF: PT101US, and myAirvo 2, REF: PT100US, used with Disinfection Kit User Manual, REF: UI-185043723 — Reason: When unintentionally disconnected from power source, humidifier device (used to deliver high flow warmed and humidified respiratory gases) may sound audible alert for less than 120 seconds, which may delay user awareness to reconnect power, which could lead to oxygen desaturation, hypoxia. Disinfection kit user manual updated to include checking the audible alert prior to use on a new patient. — Status: Ongoing

    full page →fda device recalls ↗
    ›Sep 18, 2025device recall336d agoB BRAUN MEDICAL INC device recall (Cls II)B. Braun Medical Inc

    Design Options, PERIFIX FX Epidural Anesthesia Tray. Product Code: CESK. Product Descriptions: 1. CESK ROBERT WOOD JOHNSON UNIV HOSP. 2. CESK EAST JEFFERSON GEN HOSP 20071769. 3. CESK FLETCHER ALLEN HOSPITAL. 4. CESK WASHOE MEDICAL CENTER. 5. CESK DETROIT MEDICAL CTR 20064586. 6. CESK ALBANY MEDICAL CENTER. 7. CESK EPIDURAL BLOCK TRAY. 8. CESK, BSW EPIDURAL TRAY. 9. CESK HOWARD COUNTY GENERAL. 10. CESK CE17TKFC10L. 11. CESK WILLIAMSON MEDICAL CENTER. 12. CESK FLORIDA HOSPITAL. 13. CESK RIVERSIDE HEALTH SYSTEM. 14. CESK MAYO CLINIC OB. 15. CESK PRESBYTERIAN HOSPITAL DALLAS. 16. CESK HOUSTON METHODIST HOSPITAL. 17. CESK OHIO STATE UNIV MEDICAL CENTER. 18. CESK NORTONS WOMEN'S AND CHILDREN'S. 19. CESK BEN TAUB. 20. CESK PENN MEDICINE CONTINUOUS-ORIG CUST. 21. CESK ALLEGHENY GENERAL HOSPITAL. 22. CESK UNIVERSITY OF ILLINOIS MED CTR. 23. CESK RUSH UNIVERSITY MEDICAL CENTER. 24. CESK ST. JOSEPH MEDICAL CENTER. 25. CESK INTEGRIS HEALTH. 26. CESK UMASS MEMORIAL. 27. CESK STANFORD UNIV HOSP 20054718. 28. CESK OVERLAKE HOSPITAL. 29. CESK CHRIST HOSPITAL 20057985. 30. CESK NEWTON-WELLESLEY HOSPITAL. — Reason: Potential for the lid of the catheter connector to be in the incorrect position. — Status: Ongoing

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    $CAH234.85-0.06%
    $MVIS1.7700-1.39%
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    $ABT114.43+1.55%