Drug recall
Stryker Hoffman LRF Wire Tensioner REF 4933-9-100, a component of the Hoffmann LRF System.
FDA recall event 94721 · Class II · Stryker GmbH
Key facts
| Event ID | 94721 |
|---|---|
| Recall numbers | Z-2219-2024 |
| Recalling firm | Stryker GmbH |
| Product type | Devices |
| Products | Stryker Hoffman LRF Wire Tensioner REF 4933-9-100, a component of the Hoffmann LRF System. |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | The adjustment ring on the device may become loose resulting in the wire tension not being able to be set correctly. |
| Initiation date | May 9, 2024 |
| Report date | Jul 3, 2024 |
| City | Selzach |
| Country | Switzerland |
| FEI number | 3002807830 |
At a glance
- 1–9 Products in this recall
- 1–9 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: