🔍 RecallPedia

Restrata, Part Number RWM1-2X2

Class I - Dangerous
🏥 Medical Devices Recalled: March 21, 2022 Acera Surgical Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    Lot Number 51745 UDI (01) 8 52425800 60682 (10) 51745 (17) 220218 (21) 0068
  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:
Acera Surgical Inc
Reason for Recall:
Misprinted expiration date on the shelf-box
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Restrata, Part Number RWM1-2X2

Product Codes/Lot Numbers:

Lot Number 51745 UDI (01) 8 52425800 60682 (10) 51745 (17) 220218 (21) 0068

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-1030-2022