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calendar

913 catalysts · 3,603 8k filing · 2,401 grant · 2,049 approval · 1,383 device 510k · 1,000 device adverse event · 931 device pma

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type: device recall×from 2025-11-01×clear all
type
  • 8k filing3,603
  • grant2,401
  • approval2,049
  • device 510k1,383
  • device adverse event1,000
  • device pma931
device recall
913
  • earnings585
  • recall364
  • phase 2 completion172
  • therapy area

    no tagged catalysts yet

    Week of Oct 27, 2025

    1
    ›Nov 2, 2025device recall300d agoMedtronic MiniMed, Inc. device recall (Cls II)Medtronic USA Inc

    MiniMed 780G Insulin Pump Catalog Numbers: MMT-1884 MMT-1886 With Software Version 6.60 The MiniMed 780G insulin pump is indicated for use by patients age 7-80 years with Type 1 diabetes, whose total daily dose of insulin is 8 units per day or more. The MiniMed 780G system is intended for continuous delivery of basal insulin at selectable rates, and the administration of insulin boluses at selectable amounts for the management of type 1 diabetes mellitus in persons seven years of age and older requiring insulin. The system is also intended to continuously monitor glucose values in the fluid under the skin. The MiniMed 780G system includes SmartGuard technology, which can be programmed to automatically adjust insulin delivery based on continuous glucose monitoring (CGM) sensor glucose values and can suspend delivery of insulin when the SG value falls below or is predicted to fall below predefined threshold values. — Reason: A software timing and processor communication issue in MiniMed" 780G software version 6.60 may trigger Pump Error 43 and/or Pump Error 41, resulting in suspension of insulin delivery. — Status: Ongoing

    full page →fda device recalls ↗

    Week of Nov 3, 2025

    49
    ›Nov 3, 2025device recall299d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

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

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall
    ← prev
    page 1 of 19
    next →
    299d ago
    GET TESTED INTERNATIONAL AB device recall (Cls II)

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

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall299d 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 recall299d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Organic Acids Profile Test Large — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall299d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

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

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall299d 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 recall299d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

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

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall299d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Illegally Marketed — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall299d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

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

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall299d 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 recall299d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

    Mycoplasma test, IgG and IgM — Reason: Distribution without premarket approval/clearance. — Status: Ongoing

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall299d 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 recall299d 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 recall299d 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 recall299d 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 recall299d 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 recall299d 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 recall299d 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 recall299d 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 recall299d 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

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall299d 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 recall299d 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 recall299d 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 recall299d 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 recall299d 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 recall299d 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 recall299d 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 recall299d 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 recall299d 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 recall299d 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 recall299d 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 recall299d 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 recall299d 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 recall299d 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 recall299d 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 recall299d 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 recall299d 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 recall299d 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 recall299d 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 recall299d 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 recall299d 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 recall299d 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 recall299d 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 recall299d 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 recall299d 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 recall299d 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 recall299d 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

    full page →fda device recalls ↗
    ›Nov 3, 2025device recall299d 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 recall299d agoGET TESTED INTERNATIONAL AB device recall (Cls II)

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

    full page →fda device recalls ↗