FDA Device recall Z-2875-2018
Connecting Bolt, Model 14-442093
- FDA Device
- Class II
- terminated
- Published 2018-08-29
On 2018-08-29 the FDA classified a Class II recall of Connecting Bolt, Model 14-442093 by Zimmer Biomet, citing product was manufactured from the incorrect material, which shows a potential decrease in the fatigue strength of the connecting bolt that can lead to fracture.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2875-2018 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-06-18 |
| Published | 2018-08-29 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Zimmer Biomet |
| Distribution | AR, AZ, CA, FL, GA, IN, KY, LA, MA, MI, MN, MO, MT, NJ, NY, OH, SC, TX, UT, WI |
Product
Connecting Bolt, Model 14-442093
Reason
Product was manufactured from the incorrect material, which shows a potential decrease in the fatigue strength of the connecting bolt that can lead to fracture.
Identifiers
| code_info | ... |
|---|
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-2875-2018%22
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