🔍 RecallPedia

Merete PediatrOS RigidTack, REF CP20120, Size 20 mm, Sterile, Rx Only

Class I - Dangerous
🏥 Medical Devices Recalled: January 18, 2022 Merete Medical GmbH Other Medical Devices

What Should You Do?

  1. Check if you have this product:
    Model No. CP20120; Lot No. MS2117816; UDI No. (01)04048266150394(17)260706(10)MS2117816
  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:
Merete Medical GmbH
Reason for Recall:
Incorrect marketing label (25 mm) was applied to product size 20 mm.
Classification:
Class I - Dangerous

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

Status:
terminated

Product Information

Full Description:

Merete PediatrOS RigidTack, REF CP20120, Size 20 mm, Sterile, Rx Only

Product Codes/Lot Numbers:

Model No. CP20120; Lot No. MS2117816; UDI No. (01)04048266150394(17)260706(10)MS2117816

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0650-2022

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