FDA Device recall Z-2219-2024
Stryker Hoffman LRF Wire Tensioner REF 4933-9-100, a component of the Hoffmann LRF System
- FDA Device
- Class II
- ongoing
- Published 2024-07-03
On 2024-07-03 the FDA classified a Class II recall of Stryker Hoffman LRF Wire Tensioner REF 4933-9-100, a component of the Hoffmann LRF System by Stryker, citing the adjustment ring on the device may become loose resulting in the wire tension not being able to be set correctly.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2219-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-05-09 |
| Published | 2024-07-03 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Stryker |
| Distribution | US |
Product
Stryker Hoffman LRF Wire Tensioner REF 4933-9-100, a component of the Hoffmann LRF System.
Reason
The adjustment ring on the device may become loose resulting in the wire tension not being able to be set correctly.
Identifiers
| code_info | Lot #J43995, UDI-DI 07613252611035. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2219-2024%22
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