Dual Articulating Headrest, Pad Ret P/N P141210805, REF BF754

Class I - Dangerous
🏥 Medical Devices Recalled: December 12, 2023 Steris Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    UDI-DI: 00724995197643, date of manufacture 2023-08-14 thru 2023-10-26.
  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:
Steris Corporation
Reason for Recall:
Dual-articulating head rest may not stay in place or may fail to lock into position during a patient procedure which could result in an injury to the patient or a procedural delay.
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

Dual Articulating Headrest, Pad Ret P/N P141210805, REF BF754

Product Codes/Lot Numbers:

UDI-DI: 00724995197643, date of manufacture 2023-08-14 thru 2023-10-26.

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0983-2024

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