TriMed, Threaded IM Nail 3.6mm, 60mm, TI, Ref: IMN3.6-60 T, Non Sterile, MD, Rx Only TriMed, Threaded IM Nail 3.6mm, 65mm, TI, Ref: IMN3.6-65 T, Non Sterile, MD, Rx Only
Class I - DangerousWhat Should You Do?
- Check if you have this product: UDI: 00842188127878/ Lot # QM23086
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- 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:
- Nail system contains an out of specification driver-socket which could result in inability to pick up nails or apply sufficient torque.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- ongoing
Product Information
Full Description:
TriMed, Threaded IM Nail 3.6mm, 60mm, TI, Ref: IMN3.6-60 T, Non Sterile, MD, Rx Only TriMed, Threaded IM Nail 3.6mm, 65mm, TI, Ref: IMN3.6-65 T, Non Sterile, MD, Rx Only
Product Codes/Lot Numbers:
UDI: 00842188127878/ Lot # QM23086
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-1791-2024
Related Recalls
Nail system contains an out of specification driver-socket which could result in inability to pick up nails or apply sufficient torque.
Plates, part of a wrist fixation system, are affixed during surgery with bearings that may pop out from distal peg holes.
Overly aggressive tension on the pull suture, while passing the medial button through a bone/soft tissue tunnel across the fibula and tibia, can exceed its strength causing it to break.