FDA Device recall Z-0695-2013
Hoffman LRF Wire Bolt, Catalog number 4933-1-001 through -003
- FDA Device
- Class II
- terminated
- Published 2013-01-23
On 2013-01-23 the FDA classified a Class II recall of Hoffman LRF Wire Bolt, Catalog number 4933-1-001 through -003 by Stryker Howmedica Osteonics, citing two complaints have been filed where Hoffman LRF Wires have broken during load bearing application by patients.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0695-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2012-10-25 |
| Published | 2013-01-23 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Stryker Howmedica Osteonics |
| Distribution | US |
Product
Hoffman LRF Wire Bolt, Catalog number 4933-1-001 through -003.
Reason
Two complaints have been filed where Hoffman LRF Wires have broken during load bearing application by patients.
Identifiers
| code_info | Catalog number 4933-1-001, Lot number Z02804, Z08348, Z08350, Z12549, Z16753. Catalog number 4933-1-002, Lot number Z08…Catalog number 4933-1-001, Lot number Z02804, Z08348, Z08350, Z12549, Z16753. Catalog number 4933-1-002, Lot number Z08351, Z12554, Z16246, Z16752. Catalog number 4933-1-003 Lot Number Z08349, Z09344, Z12551, Z16996. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0695-2013%22
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