Drug recall
Spinal Rod Cutter, Item number 00392500200. The product is a nonsterile pin cutter - Product Usage: The…
FDA recall event 86869 · Class II · Zimmer Biomet, Inc.
Key facts
| Event ID | 86869 |
|---|---|
| Recall numbers | Z-0696-2021 |
| Recalling firm | Zimmer Biomet, Inc. |
| Product type | Devices |
| Products | Spinal Rod Cutter, Item number 00392500200. The product is a nonsterile pin cutter - Product Usage: The intended use of this instrument is to be used for cutting orthopedic rods/pins during orthopedic… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Device has the potential for fracture during use. |
| Initiation date | Nov 20, 2020 |
| Report date | Dec 30, 2020 |
| Termination date | May 26, 2022 |
| City | Warsaw |
| State | IN |
| Country | United States |
| FEI number | 1000220733 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: