FDA Device recall Z-1526-2018
Hinge Coupling Hoffmann LRF Catalog # 4933-0-800 Intended for fixation of fractures, joint contractures, fusions, limb lengthening, deformi…
- FDA Device
- Class II
- terminated
- Published 2018-05-02
On 2018-05-02 the FDA classified a Class II recall of Hinge Coupling Hoffmann LRF Catalog # 4933-0-800 Intended for fixation of fractures, joint contractures, fusions, limb lengthening, deformi… by Stryker, citing the wrong parts were picked for packaging. The connecting Nuts were packed in the packaging labeled with Hinge coupling.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1526-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-03-12 |
| Published | 2018-05-02 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Stryker |
| Distribution | US |
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
The wrong parts were picked for packaging. The connecting Nuts were packed in the packaging labeled with Hinge coupling
Identifiers
| code_info | Lot # L23745 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1526-2018%22
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