Affixus Hip Fracture Nail, RH 130 DEG 9MM X 320MM
Class I - DangerousWhat Should You Do?
- Check if you have this product: Item No. 814509320; Lot No. (Exp. Date) UDI: 555180 (05/24/2027) UDI (01)00887868038884 (17)270524 (10)555180; 858640 (06/15/2027) UDI (01)00887868038884 (17)270615 (10)858640; 893090 (06/12/2027) UDI (01)00887868038884 (17)270612 (10)893090
- 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:
- Zimmer Biomet, Inc.
- Reason for Recall:
- During the rework process for the April 17, 2017, field action, it was detected that the set screw and sleeve assembly which are designed to have an interference fit, were no longer in the installed location. This could prevent the product assembly with the mating screw and targeting jig.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
Affixus Hip Fracture Nail, RH 130 DEG 9MM X 320MM
Product Codes/Lot Numbers:
Item No. 814509320; Lot No. (Exp. Date) UDI: 555180 (05/24/2027) UDI (01)00887868038884 (17)270524 (10)555180; 858640 (06/15/2027) UDI (01)00887868038884 (17)270615 (10)858640; 893090 (06/12/2027) UDI (01)00887868038884 (17)270612 (10)893090
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-0478-2018
Related Recalls
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