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2,005 catalysts · 18,987 approval · 5,000 device 510k · 4,876 phase readout · 4,728 grant · 2,415 8k filing · 2,000 device pma

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type: drug expiry×type: device recall×clear all
type
  • approval18,987
  • device 510k5,000
  • phase readout4,876
  • grant4,728
  • 8k filing2,415
  • device pma2,000
device recall
2,000
  • recall1,126
  • device adverse event1,000
  • earnings295
  • therapy area
    • Infectious Disease5
    • Oncology1
    • Pulmonology1

    Week of Jun 30, 2025

    50
    ›Jul 2, 2025device recall389d agoGE Medical Systems, LLC device recall (Cls II)

    GE HealthCare OEC 9900 Elite C-arm Systems. — Reason: GE HealthCare has become aware of a non-conformance to 21 CFR 1020.30 (k) in certain OEC 9800 and OEC 9900 Elite C-arm Systems. Specifically, impacted systems are missing the full layer of lead tape in the collimator covers, which will lead to a small increase in radiation exposure to the patient and/or operator. The missing lead tape is not detectable by the user. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 2, 2025device recall389d agoGE Medical Systems, LLC device recall (Cls II)

    GE HealthCare OEC 9800. — Reason: GE HealthCare has become aware of a non-conformance to 21 CFR 1020.30 (k) in certain OEC 9800 and OEC 9900 Elite C-arm Systems. Specifically, impacted systems are missing the full layer of lead tape in the collimator covers, which will lead to a small increase in radiation exposure to the patient and/or operator. The missing lead tape is not detectable by the user. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 2, 2025device recall389d agoSpark Biomedical Inc device recall (Cls II)IMPACT BIOMEDICAL INC.

    Sparrow Ascent Patient Controller, REF's: 11-110-K, 11-310-K, 11-320-K, 11-321-K, 11-310-K-28, 11-320-K-28, 11-321-K-28 — Reason: Due to manufacturing issue, neurostimulator device may experience "cable disconnect" error message and interruption to stimulation output. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall388d agoPhilips Ultrasound, Inc device recall (Cls III)

    TRANSDUCER L12-5 Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall388d agoOrascoptic Surgical Acuity device recall (Cls II)

    Orascoptic Superior Visualization Dragonfly Essentials Kit ( Nose pad, a screw, lens cleaning wipe, side shields, head strap, and a screwdriver) — Reason: Due to complaints, loupe nose pads containing nickel may cause an allergic reaction. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall388d agoPhilips Ultrasound, Inc device recall (Cls III)

    C6-2 Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall388d agoPhilips Ultrasound, Inc device recall (Cls III)

    L12-5 38mm Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall388d agoPhilips Ultrasound, Inc device recall (Cls III)

    C8-4v Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall388d agoPhilips Ultrasound, Inc device recall (Cls III)

    L9-3 Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall388d agoPhilips Ultrasound, Inc device recall (Cls III)

    X7-2 Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall388d agoTandem Diabetes Care, Inc. device recall (Cls II)TANDEM DIABETES CARE INC

    t:slim X2 Insulin Pump with Interoperable Technology (with Tandem t:slim mobile app) — Reason: an app defect that occurs when the phone is set to a right-to-left language, which causes app-pump pairing issues and graphical defects, which can potentially lead to incorrect therapy decisions and subsequent hypoglycemia or hyperglycemia. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall388d agoPhilips Ultrasound, Inc device recall (Cls III)

    S9-2 Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall388d agoPhilips Ultrasound, Inc device recall (Cls III)

    C8-5 Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall388d agoPhilips Ultrasound, Inc device recall (Cls III)

    mC7-2 Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall388d agoPhilips Ultrasound, Inc device recall (Cls III)Ocuvex Therapeutics Inc

    C5-2 Lumify Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall388d agoPhilips Ultrasound, Inc device recall (Cls III)

    X6-1 Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall388d agoPhilips Ultrasound, Inc device recall (Cls III)

    C9-3v Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall388d agoPhilips Ultrasound, Inc device recall (Cls III)

    L12-4 Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall388d agoPhilips Ultrasound, Inc device recall (Cls III)

    BP10-5ec Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall388d agoPhilips Ultrasound, Inc device recall (Cls III)

    SCNHD LA L7-4 HDI Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall388d agoPhilips Ultrasound, Inc device recall (Cls III)

    L8-4 Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall388d agoPhilips Ultrasound, Inc device recall (Cls III)

    7.5MHZ Endo Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall388d agoOrascoptic Surgical Acuity device recall (Cls II)

    Orascoptic Superior Visualization Phantom Nose Pad Accessory Kit ( nose pad and screw) 1 pk. and 20 pk. — Reason: Due to complaints, loupe nose pads containing nickel may cause an allergic reaction. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall388d agoPhilips Ultrasound, Inc device recall (Cls III)

    L10-4LAP Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall388d agoPhilips Ultrasound, Inc device recall (Cls III)

    C10-4ec Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall388d agoPhilips Ultrasound, Inc device recall (Cls III)

    X5-1 Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall388d agoPhilips Ultrasound, Inc device recall (Cls III)

    C8-4v Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall388d agoPhilips Ultrasound, Inc device recall (Cls III)

    VL13-5 Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall388d agoPhilips Ultrasound, Inc device recall (Cls III)Ocuvex Therapeutics Inc

    S4-1 Lumify Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall388d agoPhilips Ultrasound, Inc device recall (Cls III)

    S4-2 Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall388d agoPhilips Ultrasound, Inc device recall (Cls III)

    OMNI II TEE Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall388d agoPhilips Ultrasound, Inc device recall (Cls III)

    C9-2 Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall388d agoPhilips Ultrasound, Inc device recall (Cls III)

    3D9-3v Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall388d agoPhilips Ultrasound, Inc device recall (Cls III)

    L18-5 Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall388d agoPhilips Ultrasound, Inc device recall (Cls III)

    D2cwc Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall388d agoOrascoptic Surgical Acuity device recall (Cls II)

    Orascoptic Superior Visualization Dragonfly Nose Pad Accessory Kit ( nose pad and screw) 1 pk and 20 pk. — Reason: Due to complaints, loupe nose pads containing nickel may cause an allergic reaction. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall388d agoPhilips Ultrasound, Inc device recall (Cls III)

    mL26-8 Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall388d agoPhilips Ultrasound, Inc device recall (Cls III)

    C6-3 Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall388d agoPhilips Ultrasound, Inc device recall (Cls III)

    eL18-4 Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall388d agoPhilips Ultrasound, Inc device recall (Cls III)

    mC12-3 Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall388d agoPhilips Ultrasound, Inc device recall (Cls III)

    L15-7io Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall388d agoPhilips Ultrasound, Inc device recall (Cls III)

    X5-1c Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall388d agoPhilips Ultrasound, Inc device recall (Cls III)Ocuvex Therapeutics Inc

    L12-4 Lumify Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall388d agoPhilips Ultrasound, Inc device recall (Cls III)

    S7-3t Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall388d agoPhilips Ultrasound, Inc device recall (Cls III)

    S5-2 Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall388d agoPhilips Ultrasound, Inc device recall (Cls III)

    3D6-2 Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall388d agoPhilips Ultrasound, Inc device recall (Cls III)

    C9-4v Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall388d agoPhilips Ultrasound, Inc device recall (Cls III)

    S3-1 Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall388d agoPhilips Ultrasound, Inc device recall (Cls III)

    S8-3t Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
    ›Jul 3, 2025device recall388d agoPhilips Ultrasound, Inc device recall (Cls III)

    D5cwc Transducer Probe — Reason: To provide clarification and labelling to define the useful life of ultrasound transducers in the field. — Status: Ongoing

    full page →fda device recalls ↗
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