Hinge Coupling Hoffmann LRF Catalog # 4933-0-800 Intended for… — Class II medical device recall Z-1526-2018
Terminated recall by Stryker GmbH, reported 2018-05-02, distributed nationwide. The wrong parts were picked for packaging. The connecting Nuts were packed in the packaging labeled with Hinge
| Recall number | Z-1526-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Stryker GmbH, Selzach, N/A, Switzerland |
| Recall initiated | 2018-03-12 |
| Classified | 2018-04-26 |
| Reported by FDA | 2018-05-02 |
| Terminated | 2020-05-21 |
| Distributed | Nationwide (US) |
| Quantity | 18 |
| Reason classes | labeling |
| Lot numbers | L23745 |
| Model numbers | 4933-0-800 |
Product
Hinge Coupling Hoffmann LRF Catalog # 4933-0-800 Intended for fixation of fractures, joint contractures, fusions, limb lengthening, deformity correction, bone and soft tissue reconstruction in pediatric patients and adults.
Reason for recall
The wrong parts were picked for packaging. The connecting Nuts were packed in the packaging labeled with Hinge coupling
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-1526-2018. 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.