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calendar

37 catalysts · 16 device 510k · 7 recall · 6 device pma · 5 approval · 3 device recall

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Week of Jul 28, 2025

37
›Jul 30, 2025approval380d agoTRACLEER (BOSENTAN) — FDA approvalJanssen-Cilag Holdings Inc (Inactive)

Sponsor: ACTELION. Form: TABLET. Route: ORAL

full page →fda approvals ↗
›Jul 30, 2025approval380d agoTRACLEER (BOSENTAN) — FDA approvalJanssen-Cilag Holdings Inc (Inactive)

Sponsor: ACTELION. Form: TABLET, FOR SUSPENSION. Route: ORAL

full page →fda approvals ↗
›Jul 30, 2025approval380d agoACETAMINOPHEN AND CODEINE PHOSPHATE (ACETAMINOPHEN) — FDA approvalacetaminophen ER

Sponsor: CHARTWELL. Form: TABLET. Route: ORAL

full page →acetaminophen ER →fda approvals ↗
›Jul 30, 2025approval380d agoACETAMINOPHEN AND CODEINE PHOSPHATE (ACETAMINOPHEN) — FDA approvalacetaminophen ER

Sponsor: CHARTWELL. Form: TABLET. Route: ORAL

full page →acetaminophen ER →fda approvals ↗
›Jul 30, 2025approval380d agoACETAMINOPHEN AND CODEINE PHOSPHATE (ACETAMINOPHEN) — FDA approvalacetaminophen ER

Sponsor: CHARTWELL. Form: TABLET. Route: ORAL

full page →acetaminophen ER →fda approvals ↗
›Jul 30, 2025recall380d agoImprimis NJOF, LLC recall (Cls III)Sawai Man Singh Medical College

Tropicamide-Proparacaine-Phenylephrine-Ketorolac, Sterile Ophthalmic Solution, 1% 0.5% 2.5% 0.5%, 5mL, 2x5ML vial per carton, Rx Only, Imprimis NJOF, LLC, 1705 Route 46 West, Unit 6B, Ledgewood, NJ 07852, NDC 71384-733-05. — Reason: Sub-Potent Drug: Subpotent assay results during stability testing. — Status: Completed

full page →fda recalls ↗
›Jul 30, 2025recall380d agoMckesson Medical-Surgical Inc. Corporate Office recall (Cls II)AMGEN INC

EVENITY, (romosozumab -aqqg) injection, 105mg/1.17 mL, For Subcutaneous Use Only, Rx Only, Manufactured by: Amgen Inc., Thousand Oaks, CA 91320, NDC 55513-880-02. — Reason: CGMP Deviations; potential temperature excursions due to transit delays — Status: Ongoing

full page →fda recalls ↗
›Jul 30, 2025recall380d agoCipla USA, Inc. recall (Cls II)Cipla USA Inc

Budesonide Inhalation Suspension, 0.5mg/2ml, 30 single-dose ampules per carton, five per pouch, RX Only, Manufactured by: Cipla Ltd. Indore SEZ, Pithampur, India. Manufactured for: Ciple USA, Inc. 10 Independence Boulevard, Suite 300, Warren, NJ 07059. NDC# 69097-319-86 (pouch), 69097-319-87 (carton) — Reason: Lack of Assurance of Sterility: A market complaint was received for leakage and empty ampoule. — Status: Ongoing

full page →fda recalls ↗
›Jul 30, 2025recall380d agoImprimis NJOF, LLC recall (Cls II)International Medication Systems Ltd

Epinephrine Lidocaine HCL, 0.25mg/mL and 7.5 mg/mL, 20x1 mL Vials per carton, Rx Only, Imprimis NJOF, 1705 Route 46 West, Unit 6B Ledgewood, NJ, 07852 NDC: 71384-641-01 — Reason: Sub-Potent Drug: Subpotent assay results during stability testing. — Status: Completed

full page →fda recalls ↗
›Jul 30, 2025recall380d agoLupin Pharmaceuticals Inc. recall (Cls II)LB PHARMACEUTICALS INC

clomiPRAMINE Hydrochloride Capsules USP 25 mg, 100 count bottles, 5801 Pelican Bay Boulevard, Suite 500, Naples, Florida 34108, NDC# 68180-492-01 — Reason: Failed Impurities/Degradation Specifications: an out of specification result observed in degradation product test (any unspecified degradation product) during retention sample testing at expiry. — Status: Terminated

full page →fda recalls ↗
›Jul 30, 2025recall380d agoMckesson Medical-Surgical Inc. Corporate Office recall (Cls II)GSK plc

BENLYSTA (belimumab) for injection, 400 mg/20 mL vial, Rx only, NDC 49401-102-01, GSK. — Reason: CGMP Deviations; potential temperature excursions due to transit delays — Status: Ongoing

full page →fda recalls ↗
›Jul 30, 2025recall380d agoMckesson Medical-Surgical Inc. Corporate Office recall (Cls II)AMGEN INC

PROLIA (denosumab), injection, 60mg/mL, For Subcutaneous Use Only, Rx Only, Manufactured by: Amgen Inc., Thousand Oaks, CA 91320, NDC 55513-710-21 — Reason: CGMP Deviations; potential temperature excursions due to transit delays — Status: Ongoing

full page →fda recalls ↗
›Jul 30, 2025device pma380d agoCooperVision, Inc. — MiSight 1 Day (omafilcon A) Soft (Hydrophilic) Contact Lenses for Daily Wear (PMA supplement)

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

full page →fda device pma ↗
›Jul 30, 2025device pma380d agoSetPoint Medical — SetPoint System (PMA)

Product code: SFJ. Advisory committee: NE. Decision: APPR

full page →fda device pma ↗
›Jul 30, 2025device pma380d agoCentinel Spine, LLC — prodisc L (PMA supplement)

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

full page →fda device pma ↗
›Jul 30, 2025device pma380d agoBausch & Lomb, Inc. — enVista Envy™ hydrophobic acrylic intraocular lens (IOL), enVista Envy™ toric hydrophobic acrylic intraocular lens (IOL) (PMA supplement)Bausch & Lomb Corp

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

full page →fda device pma ↗
›Jul 30, 2025device pma380d agoVascutek, Ltd. — Thoraflex™ Hybrid (PMA supplement)

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

full page →fda device pma ↗
›Jul 30, 2025device pma380d agoCentinel Spine, LLC — prodisc® C (PMA supplement)

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

full page →fda device pma ↗
›Jul 30, 2025device recall380d agoMckesson Medical-Surgical Inc. Corporate Office device recall (Cls II)

Clearview Strep A Exact II Dipstick Respiratory Kit, CLIA Waived. Catalog Number: 4581225020 — Reason: Due to a classification error in the inventory management system, specific medical devices were shipped to customers that did not have the requisite license to purchase such devices. — Status: Ongoing

full page →fda device recalls ↗
›Jul 30, 2025device recall380d agoS.I.N. Implant System Ltda device recall (Cls II)

IMPLANT EPIKUT PLUS MT16 3,5X10,0MM, REF: ILM 3510N; IMPLANT EPIKUT PLUS MT16 3.8X11.5MM, REF: ILM 3511N; IMPLANT EPIKUT PLUS MT16 3,5X13,0MM, REF: ILM 3513N; IMPLANT EPIKUT PLUS MT16 3,5X15,0MM, REF: ILM 3515N; IMPLANT EPIKUT PLUS MT16 3,8X10,0MM, REF: ILM 3810N; IMPLANT CM16 3,8 X 11MM, REF: ILM 3811N; IMPLANT EPIKUT PLUS MT16 3,8X15,0MM, REF: ILM 3815N; IMPLANT EPIKUT PLUS MT16 4,0X10,0MM, REF: ILM 4010N; IMPLANT EPIKUT PLUS MT16 4,0X11,5MM, REF: ILM 4011N; IMPLANT EPIKUT PLUS MT16 4,0X13,0MM, REF: ILM 4013N; IMP EPIKUT PLUS LONG MT16 4,0X20,0MM, RES: ILM 4020N; IMPLANT EPIKUT PLUS MT16 4,0X8,5MM, RES: ILM 4085N; IMPLANT EPIKUT PLUS MT16 4,5X13,0MM, REF: ILM 4513N; IMPLANT EPIKUT PLUS MT16 4,5X15,0MM, REF: ILM 4515N; IMPLANT EPIKUT PLUS MT16 4,5X8,5MM, REF: ILM 4585N; IMPLANT EPIKUT PLUS MT16 5,0X10,0MM, REF: ILM 5010N; IMPLANT EPIKUT PLUS MT16 5,0X11,5MM, REF: ILM 5011N; IMPLANT EPIKUT PLUS MT16 4,5X10,0MM, REF: ILM 4510N; IMPLANT EPIKUT PLUS MT16 5,0X13,0MM, RES: ILM 5013N; IMPLANT EPIKUT PLUS MT16 5,0X15,0MM, REF: ILM 5015N; IMPLANT EPIKUT PLUS MT16 5,0X8,5MM, REF: ILM 5085N; IMP EPIKUT PLUS LONG MT16 4,0X18,0MM, REF: ILM 4018N; IMP EPIKUT PLUS LONG MT16 3,8X18,0MM, REF: ILM 3818N; IMPLANT EPIKUT PLUS MT16 4,5X11,5MM, REF: ILM 4511N; IMPLANT EPIKUT MT16 4,5X15,0MM, REF: ILM 4515; IMPLANT EPIKUT MT16 4,5X8,5MM, REF: ILM 4585; IMPLANT EPIKUT MT16 3,8X13,0MM, REF: ILM 3813; IMPLANT EPIKUT MT16 3,8X15,0MM, REF: ILM 3815; IMPLANT EPIKUT MT16 5,0X8,5MM, REF: ILM 5085; IMPLANT EPIKUT MT16 3,8X11,5MM, REF: ILM 3811; IMPLANT EPIKUT PLUS MT16 3,8X20,0MM, REF: ILM 3820N; IMPLANT EPIKUT PLUS MT16 4,5X18,0MM, REF: ILM 4518N; IMPLANT UNITITE MORSE COMPACT 6.0X7MM, REF: UCMC 6007N — Reason: Dental implants were imported under temperature and storage conditions that do not comply with the instructions for use and product labeling so there may be packaging damage, which could compromise product quality and performance. — Status: Ongoing

›Jul 30, 2025device recall380d agoContract Medical International GmbH device recall (Cls II)

Brand Name: Fortress Introducer Sheath System Product Name: Fortress Introducer Sheath System Model/Catalog Number: 386594 Product Description: Fortress Introducer Sheath System, 6F Straight 45cm: — Reason: Units may have been packaged with an incorrect pouch label, which lists the reference number and unique device identifier of the 4F version of the device, rather than the packaged 6F version. — Status: Ongoing

full page →fda device recalls ↗
›Jul 30, 2025device 510k380d agoShenzhen Lifotronic Technology Co., Ltd. — Diode Laser Hair Removal Machine (models: T60A, T60B, T60C, T60D, T60E) (510k cleared)

Product code: GEX. Advisory committee: General, Plastic Surgery. Type: Traditional

full page →fda device 510k ↗
›Jul 30, 2025device 510k380d agoABBOTT MEDICAL — EnSite™ X EP System (510k cleared)

Product code: DQK. Advisory committee: Cardiovascular. Type: Traditional

full page →fda device 510k ↗
›Jul 30, 2025device 510k380d agoProvidence Medical Technology, Inc. — CORUS™ Navigation System-GX (510k cleared)

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

full page →fda device 510k ↗
›Jul 30, 2025device 510k380d agoRiverpoint Medical — Iconix Speed Anchor; Iconix Speed HA+ Anchor (510k cleared)

Product code: MBI. Advisory committee: Orthopedic. Type: Special

full page →fda device 510k ↗
›Jul 30, 2025device 510k380d agoE.O.S Co., Ltd. — P-CON (polymacon) Soft (hydrophilic) Contact Lenses (Tinted, Color) (510k cleared)

Product code: LPL. Advisory committee: Ophthalmic. Type: Traditional

full page →fda device 510k ↗
›Jul 30, 2025device 510k380d agoSpectrum Vascular — Intraosseous Infusion Needles (510k cleared)

Product code: FMI. Advisory committee: General Hospital. Type: Traditional

full page →fda device 510k ↗
›Jul 30, 2025device 510k380d agoTsk Laboratory, Japan — TSK Syringe (510k cleared)

Product code: QNQ. Advisory committee: General Hospital. Type: Traditional

full page →fda device 510k ↗
›Jul 30, 2025device 510k380d agoChangsha Anxiang Medical Technology Co., Ltd. — TENS and EMS Unit (510k cleared)

Product code: NGX. Advisory committee: Physical Medicine. Type: Special

full page →fda device 510k ↗
›Jul 30, 2025device 510k380d agoHartalega NGC Sdn. Bhd. — Sterile Nitrile Powder Free Examination Glove Tested for Use with Chemotherapy Drugs and Fentanyl Citrate (Blue); Sterile Nitrile Powder Free Examination Glove Tested for Use with Chemotherapy Drugs and Fentanyl Citrate (Blue) – Extended Cuff (510k cleared)Teva Pharmaceuticals USA Inc

Product code: LZA. Advisory committee: General Hospital. Type: Traditional

full page →fda device 510k ↗
›Jul 30, 2025device 510k380d agoHermes Medical Solutions AB — Voxel Dosimetry (00859873006226) (510k cleared)

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

full page →fda device 510k ↗
›Jul 30, 2025device 510k380d agoHydrocision, Inc. — SpineSite Endoscope System (510k cleared)

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

full page →fda device 510k ↗
›Jul 30, 2025device 510k380d agoCardio Ring Technologies, Inc. Taiwan Branch — ArteVu (510k cleared)

Product code: DXN. Advisory committee: Cardiovascular. Type: Traditional

full page →fda device 510k ↗
›Jul 30, 2025device 510k380d agoTonica Elektronik A/S — T65 (9016E061-) (510k cleared)

Product code: OBP. Advisory committee: Neurology. Type: Special

full page →fda device 510k ↗
›Jul 30, 2025device 510k380d agoTyber Medical, LLC — Tyber Medical Distal Radius Plating System (510k cleared)

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

full page →fda device 510k ↗
›Jul 30, 2025device 510k380d agoSuzhou Zenith Vascular SciTech Limited — Micro Catheter (510k cleared)

Product code: KRA. Advisory committee: Cardiovascular. Type: Traditional

full page →fda device 510k ↗
›Jul 30, 2025device 510k380d agoAcuity Surgical Devices, LLC — Stabilis SA Cervical Stand-Alone System (Various PNs) (510k cleared)

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

full page →fda device 510k ↗
full page →fda device recalls ↗
$AMGN417.84+0.40%
$BLCO16.98+1.31%
$LBRX44.27-2.45%
$GSK50.45+0.30%
$AMGN417.84+0.40%