Drugs & medicalClass II

DEPUY (IRELAND) recalls Depuy Synthes, ATTUNE Revision Hinge Knee Hinge Insert Components with the below product descriptions and Part Codes. 1. ATTUNE KNEE…

The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.

Read the official notice →
Date
2026-07-08
Country
United States
Brand
Depuy
Product
Depuy Synthes, ATTUNE Revision Hinge Knee Hinge Insert Components with the below product descriptions and Part Codes. 1. ATTUNE KNEE…
Classification
Class II
Units
Distribution to MN, NC, TX.
Category
Drugs & medical
Source
FDA · Device

Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer

What to do

  1. Check the product name, strength and lot number against the official notice.
  2. Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
  3. Ask the pharmacy or supplier about a replacement or refund.

General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.

More Depuy recalls

  1. 2026-05-06
  2. US
    Drugs & medicalClass II

    DEPUY (IRELAND) recalls Depuy Synthes, ATTUNE REVISION HINGE FEMORAL LT SZ 8 CEM. Part Number: 150450108.

    The external sterile packaging was found adhered to the internal sterile packaging, potentially compromising sterility.

    FDA · DeviceDEPUY (IRELAND)US Nationwide distribution in the states of MN, NC, TX.Official notice →
All 2 Depuy recalls →

Other drugs & medical recalls in the United States

  1. 2026-07-08
  2. US
    Drugs & medicalClass II

    Remel, Inc recalls GC Agar Base (150mm) 10/PK R04030; GC Agar Base (100mm) 10/PK R01460

    Reduced or no recovery of some strains of Neisseria gonorrhoeae.

    FDA · DeviceRemel, IncWorldwide distribution - US Nationwide and the countries of Canada, Singapore,…Official notice →
  3. US
    Drugs & medicalClass I

    Windstone Medical Packaging, Inc. recalls A M S, ALIGNED MEDICAL SOLUTIONS, Dr. Lewin Pack, Pack Number AMS7200D, surgical convenience kit

    Kits contain Webcol Large Alcohol Prep Pad which were recalled by Cardinal Health following the discovery of a contaminant (Paenibacillus phoenicis) during a routine sterilization dose audit.

    FDA · DeviceWindstone Medical Packaging, Inc.US Nationwide distribution in the states of PA, GA, CA, WA.Official notice →
  4. US
    Drugs & medicalClass II

    Medacta Usa Inc recalls Short Monobloc Stem Broaches, Size/REF: 7/04.01.10.0970, 8/04.01.10.0971, 9/04.01.10.0972, 10/04.01.10.0973, 11/04.01.10.0974,…

    Surgical instruments used during shoulder arthroplasty procedures does not progressively translate to replicate implant geometry, so the reaming guide and the stem reamer are positioned approximately 0.2 mm per size…

    FDA · DeviceMedacta Usa IncUS Nationwide distribution in the states of CO, AR, IN, PA, UT, FL.Official notice →
  5. US
    Drugs & medicalClass I

    Medline Industries, LP recalls Reprocessed Electrophysiology Catheters and Ultrasound Catheters Item no. 401206RH, St. Jude Medical Response" Diagnostic…

    Expansion of RES 98277. Specific lots of reprocessed catheters may contain small particles of residual material. If devices with residual particulates on patient-contacting surfaces are used, there is a potential risk…

    FDA · DeviceMedline Industries, LPUS Nationwide distribution in the state of TX.Official notice →
  6. US
    Drugs & medicalClass II

    Mentor Texas LP recalls SYRINGE LUER LOK 10CC-200/BOX BD Product Code: 302995 Mentor Product Code: B9604 Syringe, Piston

    A single lot of expired syringes were distributed due to a distribution system control failure.

    FDA · DeviceMentor Texas LPU.S.: CA, FL, and PAOfficial notice →
  7. US
    Drugs & medicalClass II

    Medline Industries, LP recalls Medline Convenience kits containing recalled Swan-Ganz Catheters KIT GERMANTOWN CABG DYNJ905855 KIT UNIVERSITY CABG PACK DYNJ905857 OH MED…

    Kits contain Swan-Ganz catheters recalled by Becton Dickinson (BD). BD has received complaints of leaks/breakage involving failures of the (blue) proximal injectate lumen hub on these catheters. This has led to…

    FDA · DeviceMedline Industries, LPUS Nationwide distribution in the states of AZ, CA, FL, IL, MO, NJ, OH, OK,…Official notice →
See all drugs & medical recalls →