FDA Device recall Z-2251-2014
4.0 mm Cancellous Screw, Partially Threaded Sterile Zimmer
- FDA Device
- Class II
- terminated
- Published 2014-08-27
On 2014-08-27 the FDA classified a Class II recall of 4.0 mm Cancellous Screw, Partially Threaded Sterile Zimmer by Zimmer, citing zimmer is recalling various trauma screws that failed a leak test due to damage of the inner cavity only.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2251-2014 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-07-22 |
| Published | 2014-08-27 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Zimmer |
| Distribution | AK, AL, AZ, CA, CT, DC, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NJ, NM, NV, NY, OH, OK, OR, PA, PR, SC, SD, TN, TX, VA, WA, WI, WV, WY |
Product
4.0 mm Cancellous Screw, Partially Threaded Sterile Zimmer
Reason
Zimmer is recalling various trauma screws that failed a leak test due to damage of the inner cavity only.
Identifiers
| code_info | Item Number 47-4840-010, 012, 014, 016, 018, 020, 022, 024, 026, 028, 030, 035, 040, 045, 050, 055, 060, 065, 070, 075, 080, 085, 090, 095, 100-01 |
|---|
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-2251-2014%22
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