Recall Z-2593-2017 ยท KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component
Zimmer Biomet, Inc.
VERSA-FXII SC TUBE PLT 90DX16H, 95DX16H, 95DX18H, 95DX20H, 95DX22H
| Date | Apr 28, 2017 |
| Status | Terminated |
| Reason | Zimmer Biomet is initiating a field action for sterile-packaged implants packaged in a single package configuration due to packaging design verification test failures. |
| Root cause | Under Investigation by firm |
| Action | Zimmer Biomet initiated a voluntary recall for sterile-packaged implants packaged in a single package configuration due to packaging design verification test failures. Compromised packaging may result in surgical delays, possible infections, and revision surgeries due to infections. The firm distributed letters to customer via FED EX on 04/28/2017. Customers were instructed to do the following: 1. Review this notification and ensure affected personnel are aware of the contents. 2. Immediately locate and quarantine affected product in your inventory. 3. Complete the Certification of Acknow |
| Quantity | 445 |
| Distribution | Domestic: Puerto Rico, AK AL AR AZ CA CO CT FL GA HI IA ID IL IN KS KY LA MA MD ME MI MN MO MS MT NC ND NE NH NJ NM NV NY OH OK OR PA RI SC SD TN TX UT VA VT WA WI WV WY Foreign: CANADA, ALGERIA ARGENTINA AUSTRALIA |
| FDA record | Open on fda.gov |
510(k) clearances named in this recall
| K830196 | CORSTREN COMPRESSION TUBE & PLATE Zimmer, Inc., Mar 25, 1983 |