🔍 RecallPedia

REF: 60-7070-005, Zimmer, Tourniquet Cuff 30" (Blue), Luer-Lock Dual Port, single Bladder, RxOnly

Class I - Dangerous
🏥 Medical Devices Recalled: May 31, 2024 Stryker Sustainability Solutions Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    Lot: 0000564862/ UDI: 00885825015411
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Stryker Sustainability Solutions
Reason for Recall:
Mislabeling; tourniquet cuff packaging labeled as dual port single bladder but contains a tourniquet cuff single port single bladder.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
ongoing

Product Information

Full Description:

REF: 60-7070-005, Zimmer, Tourniquet Cuff 30" (Blue), Luer-Lock Dual Port, single Bladder, RxOnly

Product Codes/Lot Numbers:

Lot: 0000564862/ UDI: 00885825015411

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-2405-2024

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Disposable 5 Lead Cable and Lead Wire System, 50 inches, REF: LW-309DS50/5A

Stryker Sustainability Solutions

Class I - Dangerous

Disposable 5 lead cable and lead wire system package that should contain lead systems, lead telemetry systems and a dual connect cable, may in fact contain, different ECG Leads, which are not approved for reprocessing, but that may have been reprocessed, which may lead to devices not performing as intended.

Jul 2, 2024 Other Medical Devices Nationwide View Details →