TriMed Peg Guide Extender, REF PEG-XTNDR, nonsterile, Rx. The firm name on the label is TriMed Inc., Santa Clarita, CA.

Class I - Dangerous
🏥 Medical Devices Recalled: September 28, 2018 TriMed Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    Lot number 2858, 2861, and 3749
  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:
TriMed Inc.
Reason for Recall:
The spring on the PEG-Extender can rust due to the type of steel used to manufacture it.
Classification:
Class I - Dangerous

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

Status:
ongoing

Product Information

Full Description:

TriMed Peg Guide Extender, REF PEG-XTNDR, nonsterile, Rx. The firm name on the label is TriMed Inc., Santa Clarita, CA.

Product Codes/Lot Numbers:

Lot number 2858, 2861, and 3749

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0358-2020

Related Recalls

Plates, part of a wrist fixation system, are affixed during surgery with bearings that may pop out from distal peg holes.

Nov 28, 2023 Other Medical Devices View Details →