FDA Device recall Z-2744-2015
Biomet Parsippany, NJ. 4 0 MM X 14 MM Variable Screw C-Tek Maxan Anterior Cervical Plate System
- FDA Device
- Class II
- terminated
- Published 2015-09-16
On 2015-09-16 the FDA classified a Class II recall of Biomet Parsippany, NJ. 4 0 MM X 14 MM Variable Screw C-Tek Maxan Anterior Cervical Plate System by Biomet Spine, citing some of P/N 14-521614B Lot 375440 was mislabeled as P/N 14-521614 Lot 375440.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2744-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2015-08-05 |
| Published | 2015-09-16 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Biomet Spine |
| Distribution | US |
Product
Biomet Parsippany, NJ. 4 0 MM X 14 MM Variable Screw C-Tek Maxan Anterior Cervical Plate System. Lot 375440.
Reason
Some of P/N 14-521614B Lot 375440 was mislabeled as P/N 14-521614 Lot 375440.
Identifiers
| code_info | Model Number 14-521614B, lot number 375440. |
|---|
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-2744-2015%22
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