TriMed Hex Driver 1.2, 55mm AO Cannulated, REF HXDRIVR-1.2C AO, nonsterile, Rx. The firm name on the label is TriMed Inc., Santa Clarita, CA.
Class I - DangerousWhat Should You Do?
- Check if you have this product: Lot numbers 91500604 and 91600017
- 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:
- The epoxy on Apex manufactured epoxy-coated instruments can pop off.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- ongoing
Product Information
Full Description:
TriMed Hex Driver 1.2, 55mm AO Cannulated, REF HXDRIVR-1.2C AO, nonsterile, Rx. The firm name on the label is TriMed Inc., Santa Clarita, CA.
Product Codes/Lot Numbers:
Lot numbers 91500604 and 91600017
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-0357-2020
Related Recalls
Nail system contains an out of specification driver-socket which could result in inability to pick up nails or apply sufficient torque.
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.