Arthrex Suture Washer

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    Unique Device Identifier (UDI): 00888867118607; Catalog # AR-7000-18T; Batch #10028617.
  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:
Arthrex, Inc.
Reason for Recall:
The device was assembled incorrectly. Suture and washer were not assembled; components were placed loose in the package.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Arthrex Suture Washer

Product Codes/Lot Numbers:

Unique Device Identifier (UDI): 00888867118607; Catalog # AR-7000-18T; Batch #10028617.

Distribution:

Distributed in: OR, NY, MN, KY, CA, ID, CO, MA, FL

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-2918-2016

Related Recalls