Drug recall
Hoffman LRF Wire Bolt, Catalog number 4933-1-001 through -003.
FDA recall event 63863 · Class II · Stryker Howmedica Osteonics Corp.
Key facts
| Event ID | 63863 |
|---|---|
| Recall numbers | Z-0695-2013 |
| Recalling firm | Stryker Howmedica Osteonics Corp. |
| Product type | Devices |
| Products | Hoffman LRF Wire Bolt, Catalog number 4933-1-001 through -003. |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Two complaints have been filed where Hoffman LRF Wires have broken during load bearing application by patients. |
| Initiation date | Oct 25, 2012 |
| Report date | Jan 23, 2013 |
| Termination date | Dec 1, 2015 |
| City | Mahwah |
| State | NJ |
| Country | United States |
| FEI number | 3003070421 |
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: