Stryker Hoffman LRF Wire Tensioner REF 4933-9-100 — Class II medical device recall Z-2219-2024
Ongoing recall by Stryker GmbH, reported 2024-07-03, distributed nationwide. The adjustment ring on the device may become loose resulting in the wire tension not being able to be set corr
| Recall number | Z-2219-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Stryker GmbH, Selzach, Switzerland |
| Recall initiated | 2024-05-09 |
| Classified | 2024-06-27 |
| Reported by FDA | 2024-07-03 |
| Distributed | Nationwide (US) |
| Countries outside the US | DE, GB, JP, NL |
| Quantity | 39 devices |
| UPC / GTIN / UDI-DI | 07613252611035 |
| Lot numbers | J43995 |
| Model numbers | 4933-9-100 |
Product
Stryker Hoffman LRF Wire Tensioner REF 4933-9-100, a component of the Hoffmann LRF System.
Reason for recall
The adjustment ring on the device may become loose resulting in the wire tension not being able to be set correctly.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2219-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.