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2,000 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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2026-07-27: 2 catalysts2026-07-28: 4 catalysts2026-07-29: 12 catalysts2026-07-30: 12 catalysts2026-07-31: 3 catalysts2026-08-01: 0 catalysts2026-08-02: 0 catalysts2026-08-03: 4 catalysts2026-08-04: 12 catalysts2026-08-05: 14 catalysts2026-08-06: 10 catalysts2026-08-07: 1 catalyst2026-08-08: 0 catalysts2026-08-09: 0 catalysts2026-08-10: 1 catalyst2026-08-11: 1 catalyst2026-08-12: 1 catalyst2026-08-13: 0 catalysts2026-08-14: 0 catalysts2026-08-15: 0 catalysts2026-08-16: 0 catalysts2026-08-17: 0 catalysts2026-08-18: 1 catalyst2026-08-19: 0 catalysts2026-08-20: 0 catalysts2026-08-21: 0 catalysts2026-08-22: 0 catalysts2026-08-23: 0 catalysts2026-08-24: 0 catalysts2026-08-25: 0 catalysts2026-08-26: 0 catalysts2026-08-27: 0 catalysts2026-08-28: 0 catalysts2026-08-29: 0 catalysts2026-08-30: 0 catalysts2026-08-31: 0 catalysts2026-09-01: 1 catalyst2026-09-02: 0 catalysts2026-09-03: 0 catalysts2026-09-04: 0 catalysts2026-09-05: 0 catalysts2026-09-06: 0 catalysts2026-09-07: 0 catalysts2026-09-08: 0 catalysts2026-09-09: 0 catalysts2026-09-10: 0 catalysts2026-09-11: 0 catalysts2026-09-12: 0 catalysts2026-09-13: 0 catalysts2026-09-14: 0 catalysts2026-09-15: 0 catalysts2026-09-16: 0 catalysts2026-09-17: 0 catalysts2026-09-18: 0 catalysts2026-09-19: 0 catalysts2026-09-20: 0 catalysts2026-09-21: 0 catalysts2026-09-22: 0 catalysts2026-09-23: 0 catalysts2026-09-24: 0 catalysts2026-09-25: 0 catalysts2026-09-26: 0 catalysts2026-09-27: 0 catalysts2026-09-28: 0 catalysts2026-09-29: 0 catalysts2026-09-30: 0 catalysts2026-10-01: 0 catalysts2026-10-02: 0 catalysts2026-10-03: 0 catalysts2026-10-04: 0 catalysts2026-10-05: 0 catalysts2026-10-06: 0 catalysts2026-10-07: 0 catalysts2026-10-08: 0 catalysts2026-10-09: 0 catalysts2026-10-10: 0 catalysts2026-10-11: 0 catalysts2026-10-12: 0 catalysts2026-10-13: 0 catalysts2026-10-14: 0 catalysts2026-10-15: 0 catalysts2026-10-16: 0 catalysts2026-10-17: 0 catalysts2026-10-18: 0 catalysts2026-10-19: 0 catalysts2026-10-20: 1 catalyst2026-10-21: 0 catalysts2026-10-22: 1 catalyst2026-10-23: 0 catalysts2026-10-24: 0 catalysts2026-10-25: 0 catalysts
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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

    no tagged catalysts yet

    Week of Nov 3, 2025

    50
    ›Nov 3, 2025device recall266d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Adrenal Test — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall266d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Neurotransmitters Plus — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall266d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Pollen Allergy Test — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall266d agoFresenius Kabi USA, LLC device recall (Cls II)Fresenius Kabi USA LLC

    Ivenix Infusion System (IIS), Large Volume Pump. Model Number: LVP-0004. — Reason: Downstream Occlusion alarms may occur during procedures using low flow infusion rates when a check valve* is added to the Ivenix Administration Set. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall266d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Alcohol (ALC) Test Saliva — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall266d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Gut Microbiome Test XL — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall266d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Pet Allergy Test — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall266d agoOrthofix U.S. LLC device recall (Cls III)

    Brand Name: Forza" Ti Spacer System Product Name: Forza" Ti Spacer System Model/Catalog Number: 38-2006SP FORZA Ti Spacer, Straight, 0¿, 9W x 23L x 6H; 38-2007SP FORZA Ti Spacer, Straight, 0¿, 9W x 23L x 7H; 38-2008SP FORZA Ti Spacer, Straight, 0¿, 9W x 23L x 8H; 38-2009SP FORZA Ti Spacer, Straight, 0¿, 9W x 23L x 9H; 38-2010SP FORZA Ti Spacer, Straight, 0¿, 9W x 23L x 10H; 38-2011SP FORZA Ti Spacer, Straight, 0¿, 9W x 23L x 11H; 38-2012SP FORZA Ti Spacer, Straight, 0¿, 9W x 23L x 12H; 38-2013SP FORZA Ti Spacer, Straight, 0¿, 9W x 23L x 13H; 38-2014SP FORZA Ti Spacer, Straight, 0¿, 9W x 23L x 14H; 38-2106SP FORZA Ti Spacer, Straight, 0¿, 9W x 27L x 6H; 38-2107SP FORZA Ti Spacer, Straight, 0¿, 9W x 27L x 7H; 38-2108SP FORZA Ti Spacer, Straight, 0¿, 9W x 27L x 8H; 38-2109SP FORZA Ti Spacer, Straight, 0¿, 9W x 27L x 9H; 38-2110SP FORZA Ti Spacer, Straight, 0¿, 9W x 27L x 10H; 38-2111SP FORZA Ti Spacer, Straight, 0¿, 9W x 27L x 11H; 38-2112SP FORZA Ti Spacer, Straight, 0¿, 9W x 27L x 12H; 38-2113SP FORZA Ti Spacer, Straight, 0¿, 9W x 27L x 13H; 38-2114SP FORZA Ti Spacer, Straight, 0¿, 9W x 27L x 14H; 38-2206SP FORZA Ti Spacer, Straight, 0¿, 11W x 27L x 6H; 38-2207SP FORZA Ti Spacer, Straight, 0¿, 11W x 27L x 7H; 38-2208SP FORZA Ti Spacer, Straight, 0¿, 11W x 27L x 8H; 38-2209SP FORZA Ti Spacer, Straight, 0¿, 11W x 27L x 9H; 38-2210SP FORZA Ti Spacer, Straight, 0¿, 11W x 27L x 10H; 38-2211SP FORZA Ti Spacer, Straight, 0¿, 11W x 27L x 11H; 38-2212SP FORZA Ti Spacer, Straight, 0¿, 11W x 27L x 12H; 38-2213SP FORZA Ti Spacer, Straight, 0¿, 11W x 27L x 13H; 38-2214SP FORZA Ti Spacer, Straight, 0¿, 11W x 27L x 14H; 38-2309SP FORZA Ti Spacer, Straight, 8¿, 11W x 27L x 9H; 38-2310SP FORZA Ti Spacer, Straight, 8¿, 11W x 27L x 10H; 38-2311SP FORZA Ti Spacer, Straight, 8¿, 11W x 27L x 11H; 38-2312SP FORZA Ti Spacer, Straight, 8¿, 11W x 27L x 12H; 38-2313SP FORZA Ti Spacer, Straight, 8¿, 11W x 27L x 13H; 38-2314SP FORZA Ti Spacer, Straight, 8¿, 11W x 27L x 14H; 38-2508SP FORZA Ti Spacer, Straight, 8¿, 9W x 23L x 8H; 38-2509SP FORZA Ti Spacer, Straight, 8¿, 9W x 23L x 9H; 38-2510SP FORZA Ti Spacer, Straight, 8¿, 9W x 23L x 10H; 38-2511SP FORZA Ti Spacer, Straight, 8¿, 9W x 23L x 11H; 38-2512SP FORZA Ti Spacer, Straight, 8¿, 9W x 23L x 12H; 38-2513SP FORZA Ti Spacer, Straight, 8¿, 9W x 23L x 13H; 38-2514SP FORZA Ti Spacer, Straight, 8¿, 9W x 23L x 14H; 38-3206SP FORZA Ti Spacer, Straight, 0¿, 11W x 31L x 6H; 38-3207SP FORZA Ti Spacer, Straight, 0¿, 11W x 31L x 7H; 38-3208SP FORZA Ti Spacer, Straight, 0¿, 11W x 31L x 8H; 38-3209SP FORZA Ti Spacer, Straight, 0¿, 11W x 31L x 9H; 38-3210SP FORZA Ti Spacer, Straight, 0¿, 11W x 31L x 10H; 38-3211SP FORZA Ti Spacer, Straight, 0¿, 11W x 31L x 11H; 38-3212SP FORZA Ti Spacer, Straight, 0¿, 11W x 31L x 12H; 38-3213SP FORZA Ti Spacer, Straight, 0¿, 11W x 31L x 13H; 38-3214SP FORZA Ti Spacer, Straight, 0¿, 11W x 31L x 14H; 38-3409SP FORZA Ti Spacer, Straight, 8¿, 11W x 31L x 9H; 38-3410SP FORZA Ti Spacer, Straight, 8¿, 11W x 31L x 10H; 38-3411SP FORZA Ti Spacer, Straight, 8¿, 11W x 31L x 11H; 38-3412SP FORZA Ti Spacer, Straight, 8¿, 11W x 31L x 12H; — Reason: Labeling contains claims that are not consistently present. — Status: Ongoing

    ›Nov 3, 2025device recall266d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Urinary Tract Infection Test — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall266d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Lactose Intolerance Test — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall266d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    PSA Test — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall266d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Gut Microbiome Test Small — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall266d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    8 in 1 STI Test Kit — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall266d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Akkermansia Test — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall266d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Food Intolerance Test Medium — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall266d agoGE Healthcare GmbH device recall (Cls II)

    GE HealthCare ViewPoint 6, Catalog Number H47601AA; Radiological image processing system — Reason: GE HealthCare has become aware that the Patient History tab in ViewPoint 6 versions 6.15.3 and 6.15.4 ultrasound software may not include complete patient medical history information. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall266d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Food Sensitivity Test Large — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall266d agoFresenius Kabi USA, LLC device recall (Cls I)Fresenius Kabi USA LLC

    IVENIX INFUSION SYSTEM, LVP Primary Administration Set, Dual-Inlet, Low-Sorbing, Needle-Free Port, Dual Y-Site (Qty 25). Large Volume Infusion Pump Administration Set. — Reason: Incorrect assembly of specific lot of LVP Primary Administration Set that could result in serious patient injury. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall266d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Mycotoxin Panel Test — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall266d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Food Sensitivity Test Small — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall266d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Allergy test Small — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall266d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Peptic Ulcer Test (H, pylori) — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall266d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Heavy Metals Test — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall266d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Fructose Intolerance Test — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall266d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Trichomonas Vaginalis test — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall266d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    SIBO Test — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall266d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Intestinal Worms Test — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall266d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    D-Dimer Test — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall266d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Diabetes HbA1c Test — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall266d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Candida Test — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall266d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Syphilis Test — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall266d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Iodine Test — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall266d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    MPOX Test — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall266d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    GI Microbiome Profile Small — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall266d agoOrthofix U.S. LLC device recall (Cls III)

    Brand Name: CONSTRUX" Mini Ti Spacer System Product Name: CONSTRUX" Mini Ti Spacer System Model/Catalog Number: 37-6005SP 12mm W X 12mm L, 5mm H, 5¿ Lordotic 37-6005SP 12mm W X 12mm L, 5mm H, 5¿ Lordotic 37-6005SP 12mm W X 12mm L, 5mm H, 5¿ Lordotic 37-6006SP 12mm W X 12mm L, 6mm H, 5¿ Lordotic 37-6006SP 12mm W X 12mm L, 6mm H, 5¿ Lordotic 37-6006SP 12mm W X 12mm L, 6mm H, 5¿ Lordotic 37-6007SP 12mm W X 12mm L, 7mm H, 5¿ Lordotic 37-6007SP 12mm W X 12mm L, 7mm H, 5¿ Lordotic 37-6007SP 12mm W X 12mm L, 7mm H, 5¿ Lordotic 37-6008SP 12mm W X 12mm L, 8mm H, 5¿ Lordotic 37-6008SP 12mm W X 12mm L, 8mm H, 5¿ Lordotic 37-6008SP 12mm W X 12mm L, 8mm H, 5¿ Lordotic 37-6009SP 12mm W X 12mm L, 9mm H, 5¿ Lordotic 37-6009SP 12mm W X 12mm L, 9mm H, 5¿ Lordotic 37-6009SP 12mm W X 12mm L, 9mm H, 5¿ Lordotic 37-6010SP 12mm W X 12mm L, 10mm H, 5¿ Lordotic 37-6010SP 12mm W X 12mm L, 10mm H, 5¿ Lordotic 37-6010SP 12mm W X 12mm L, 10mm H, 5¿ Lordotic 37-6011SP 12mm W X 12mm L, 11mm H, 5¿ Lordotic 37-6011SP 12mm W X 12mm L, 11mm H, 5¿ Lordotic 37-6011SP 12mm W X 12mm L, 11mm H, 5¿ Lordotic 37-6012SP 12mm W X 12mm L, 12mm H, 5¿ Lordotic 37-6012SP 12mm W X 12mm L, 12mm H, 5¿ Lordotic 37-6012SP 12mm W X 12mm L, 12mm H, 5¿ Lordotic 37-6105SP 12mm W X 12mm L, 5mm H, Parallel 37-6105SP 12mm W X 12mm L, 5mm H, Parallel 37-6105SP 12mm W X 12mm L, 5mm H, Parallel 37-6106SP 12mm W X 12mm L 6mm H, Parallel 37-6106SP 12mm W X 12mm L 6mm H, Parallel 37-6106SP 12mm W X 12mm L 6mm H, Parallel 37-6107SP 12mm W X 12mm L, 7mm H, Parallel 37-6107SP 12mm W X 12mm L, 7mm H, Parallel 37-6107SP 12mm W X 12mm L, 7mm H, Parallel 37-6108SP 12mm W X 12mm L, 8mm H, Parallel 37-6108SP 12mm W X 12mm L, 8mm H, Parallel 37-6108SP 12mm W X 12mm L, 8mm H, Parallel 37-6109SP 12mm W X 12mm L, 9mm H, Parallel 37-6109SP 12mm W X 12mm L, 9mm H, Parallel 37-6109SP 12mm W X 12mm L, 9mm H, Parallel 37-6110SP 12mm W X 12mm L, 10mm H, Parallel 37-6110SP 12mm W X 12mm L, 10mm H, Parallel 37-6110SP 12mm W X 12mm L, 10mm H, Parallel 37-6111SP 12mm W X 12mm L, 11mm H, Parallel 37-6111SP 12mm W X 12mm L, 11mm H, Parallel 37-6111SP 12mm W X 12mm L, 11mm H, Parallel 37-6112SP 12mm W X 12mm L, 12mm H, Parallel 37-6112SP 12mm W X 12mm L, 12mm H, Parallel 37-6112SP 12mm W X 12mm L, 12mm H, Parallel 37-6206SP 12mm W X 12mm L, 6mm H, 10¿ Lordotic 37-6206SP 12mm W X 12mm L, 6mm H, 10¿ Lordotic 37-6206SP 12mm W X 12mm L, 6mm H, 10¿ Lordotic 37-6207SP 12mm W X 12mm L, 7mm H, 10¿ Lordotic 37-6207SP 12mm W X 12mm L, 7mm H, 10¿ Lordotic 37-6207SP 12mm W X 12mm L, 7mm H, 10¿ Lordotic 37-6208SP 12mm W X 12mm L, 8mm H, 10¿ Lordotic 37-6208SP 12mm W X 12mm L, 8mm H, 10¿ Lordotic 37-6208SP 12mm W X 12mm L, 8mm H, 10¿ Lordotic 37-6209SP 12mm W X 12mm L, 9mm H, 10¿ Lordotic 37-6209SP 12mm W X 12mm L, 9mm H, 10¿ Lordotic 37-6209SP 12mm W X 12mm L, 9mm H, 10¿ Lordotic 37-6210SP 12mm W X 12mm L, 10mm H, 10¿ Lordotic 37-6210SP 12mm W X 12mm L, 10mm H, 10¿ Lordotic 37-6210SP 12mm W X 12mm L, 10mm H, 10¿ Lordotic 37-6211SP 12mm W X 12mm L, 11mm H, 10¿ Lordotic 37-6211SP 12mm W X 12mm L, 11mm H, 10¿ Lordotic 37-6211SP 12mm W X 12mm L, 11mm H, 10¿ Lordotic — Reason: Labeling contains claims that are not consistently present. — Status: Ongoing

    ›Nov 3, 2025device recall266d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Parasite Test — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall266d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Sperm Test — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall266d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    DHEA Test — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall266d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Serotonin Test — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall266d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Female Fertility Test — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall266d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Gut Microbiome Test Mega — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall266d agoOrthofix U.S. LLC device recall (Cls III)

    Brand Name: CONSTRUX" Mini PTC Spacer System Product Name: CONSTRUX" Mini PTC Spacer System Model/Catalog Number: 37-3106SP 12mm W X 12mm L, 6mm H, Parallel; 37-3107SP 12mm W X 12mm L, 7mm H, Parallel; 37-3108SP 12mm W X 12mm L, 8mm H, Parallel; 37-3109SP 12mm W X 12mm L, 9mm H, Parallel; 37-3110SP 12mm W X 12mm L, 10mm H, Parallel; 37-3111SP 12mm W X 12mm L, 11mm H, Parallel; 37-3112SP 12mm W X 12mm L, 12mm H, Parallel; 37-3113SP 12mm W X 12mm LW, 13mm H, Parallel; 37-3114SP 12mm W X 12mm WL, 14mm H, Parallel; 37-3006SP 12mm W X 12mm L, 6mm H, 5¿ Lordotic; 37-3007SP 12mm W X 12mm L, 7mm H, 5¿ Lordotic; 37-3008SP 12mm W X 12mm L, 8mm H, 5¿ Lordotic; 37-3009SP 12mm WL X 12mm L, 9mm H, 5¿ Lordotic; 37-3010SP 12mm W X 12mm L, 10mm H, 5¿ Lordotic; 37-3011SP 12mm W X 12mm L, 11mm H, 5¿ Lordotic; 37-3012SP 12mm W X 12mm L, 12mm H, 5¿ Lordotic; 37-3013SP 12mm W X 12mm L, 13mm H, 5¿ Lordotic; 37-3014SP 12mm W X 12mm L, 14mm H, 5¿ Lordotic; 37-3207SP 12mm W X 12mm L, 7mm H, 10¿ Lordotic; 37-3208SP 12mm W X 12mm L, 8mm H, 10¿ Lordotic; 37-3209SP 12mm W X 12mm L, 9mm H, 10¿ Lordotic; 37-3210SP 12mm W X 12mm L, 10mm H, 10¿ Lordotic; 37-3211SP 12mm W X 12mm L, 11mm H, 10¿ Lordotic; 37-3212SP 12mm W X 12mm L, 12mm H, 10¿ Lordotic; 37-4106SP 15mm W X 12mm L, 6mm H, Parallel; 37-4107SP 15mm W X 12mm L, 7mm H, Parallel; 37-4108SP 15mm W X 12mm L, 8mm H, Parallel; 37-4109SP 15mm W X 12mm L, 9mm H, Parallel; 37-4110SP 15mm W X 12mm L, 10mm H, Parallel; 37-4111SP 15mm W X 12mm L, 11mm H, Parallel; 37-4112SP 15mm W X 12mm L, 12mm H, Parallel; 37-4113SP 15mm W X 12mm L, 13mm H, Parallel; 37-4114SP 15mm W X 12mm L, 14mm H, Parallel; 37-4006SP 15mm W X 12mm L, 6mm H, 5¿ Lordotic; 37-4007SP 15mm W X 12mm L, 7mm H, 5¿ Lordotic; 37-4008SP 15mm W X 12mm L, 8mm H, 5¿ Lordotic; 37-4009SP 15mm W X 12mm L, 9mm H, 5¿ Lordotic; 37-4010SP 15mm W X 12mm L, 10mm H, 5¿ Lordotic; 37-4011SP 15mm W X 12mm L, 11mm H, 5¿ Lordotic; 37-4012SP 15mm W X 12mm L, 12mm H, 5¿ Lordotic; 37-4013SP 15mm W X 12mm L, 13mm H, 5¿ Lordotic; 37-4014SP 15mm W X 12mm L, 14mm H, 5¿ Lordotic; 37-4207SP 15mm W X 12mm L, 7mm H, 10¿ Lordotic; 37-4208SP 15mm W X 12mm L, 8mm H, 10¿ Lordotic; 37-4209SP 15mm W X 12mm L, 9mm H, 10¿ Lordotic; 37-4210SP 15mm W X 12mm L, 10mm H, 10¿ Lordotic; 37-4211SP 15mm W X 12mm L, 11mm H, 10¿ Lordotic; 37-4212SP 15mm W X 12mm L, 12mm H, 10¿ Lordotic; 37-5106SP 15mm W X 15mm L, 6mm H, Parallel; 37-5107SP 15mm W X 15mm L, 7mm H, Parallel 37-5108SP 15mm W X 15mm L, 8mm H, Parallel; 37-5109SP 15mm W X 15mm L, 9mm H, Parallel; 37-5110SP 15mm W X 15mm L, 10mm H, Parallel; 37-5111SP 15mm W X 15mm L, 11mm H, Parallel; 37-5112SP 15mm W X 15mm L, 12mm H, Parallel; 37-5113SP 15mm W X 15mm L, 13mm H, Parallel; 37-5114SP 15mm W X 15mm L, 14mm H, Parallel; 37-5006SP 15mm W X 15mm L, 6mm H, 5¿ Lordotic; 37-5007SP 15mm W X 15mm L, 7mm H, 5¿ Lordotic; 37-5008SP 15mm W X 15mm L, 8mm H, 5¿ Lordotic; 37-5009SP 15mm W X 15mm L, 9mm H, 5¿ Lordotic; 37-5010SP 15mm W X 15mm L, 10mm H, 5¿ Lordotic; 37-5011SP 15mm W X 15mm L, 11mm H, 5¿ Lordotic; 37-5012SP 15mm W X 15mm L, 12mm H, 5¿ Lordotic; 37-5013SP 15mm W X 15mm L, 13mm H, 5¿ Lordotic; 37-5014SP 15mm W X 15mm L, 14mm H, 5¿ Lordotic; 37-5207SP 15mm W X 15mm L, 7mm H, 10¿ Lordotic; 37-5208SP 15mm W X 15mm L, 8mm H, 10¿ Lordotic; 37-5209SP 15mm W X 15mm LW, 9mm H, 10¿ Lordotic; 37-5210SP 15mm W X 15mm L, 10mm H, 10¿ Lordotic; 37-5211SP 15mm W X 15mm L, 11mm H, 10¿ Lordotic; 37-5212SP 15mm W X 15mm L, 12mm H, 10¿ Lordotic; — Reason: Labeling contains claims that are not consistently present. — Status: Ongoing

    ›Nov 3, 2025device recall266d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Food Allergy Panel Test (IgE) — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall266d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Food Intolerance Test Large — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall266d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    NAD Profile Test — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

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    ›Nov 3, 2025device recall266d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Vitamin D2 and D3 Test — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall266d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Leaky Gut Test — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

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    ›Nov 3, 2025device recall266d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Kidney Test — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall266d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    2 in 1 Trichomonas / Gardnerella Test — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall266d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Menopause (FSH) 2 Tests — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

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