FDA Device recall Z-0406-2014
Synthes 2.4 mm LC-DCP Plate 6 Holes/51mm Product Usage: Intended for fractures, osteotomies, and replantations of small bones including the…
- FDA Device
- Class II
- terminated
- Published 2013-12-04
On 2013-12-04 the FDA classified a Class II recall of Synthes 2.4 mm LC-DCP Plate 6 Holes/51mm Product Usage: Intended for fractures, osteotomies, and replantations of small bones including the… by Synthes Usa Products, citing A complaint was reported regarding a screw being found in a package labeled for 2.4 mm LC-DCP Plate.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0406-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-07-30 |
| Published | 2013-12-04 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Synthes Usa Products |
| Distribution | US |
Product
Synthes 2.4 mm LC-DCP Plate 6 Holes/51mm Product Usage: Intended for fractures, osteotomies, and replantations of small bones including the foot, ankle, and hand.
Reason
A complaint was reported regarding a screw being found in a package labeled for 2.4 mm LC-DCP Plate.
Identifiers
| code_info | Part No. 249.926, lot No. 8093100 |
|---|
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-0406-2014%22
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