1) ACS Arthroscopy Kit 2) ACS Knee Kit 3) ACS Hand Pack

Class I - Dangerous

What Should You Do?

  1. Check if you have this product:
    1) ACS Arthroscopy Kit - Model LMAR15R, Lot 981221; UDI: 00191072152978 2) ACS Knee Kit - Model LWKN46N, Lot 966221; UDI: 00191072150158 3) ACS Hand Pack - Model FHHP63T, Lot 966221, UDI: 00191072149954
  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:
American Contract Systems, Inc.
Reason for Recall:
Product was sterilized with a higher than specification EO concentration.
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

1) ACS Arthroscopy Kit 2) ACS Knee Kit 3) ACS Hand Pack

Product Codes/Lot Numbers:

1) ACS Arthroscopy Kit - Model LMAR15R, Lot 981221; UDI: 00191072152978 2) ACS Knee Kit - Model LWKN46N, Lot 966221; UDI: 00191072150158 3) ACS Hand Pack - Model FHHP63T, Lot 966221, UDI: 00191072149954

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1037-2022

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