Magna-Fx Cannulated Screw Fixation System Cannulated Bone Screw… — Class II medical device recall Z-2245-2014
Terminated recall by Zimmer, Inc., reported 2014-08-27, distributed in AK, AL, AZ, CA, CT, DC, FL, GA…. Zimmer is recalling various trauma screws that failed a leak test due to damage of the inner cavity only.
| Recall number | Z-2245-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zimmer, Inc., Warsaw, IN, United States |
| Recall initiated | 2014-07-22 |
| Classified | 2014-08-15 |
| Reported by FDA | 2014-08-27 |
| Terminated | 2015-06-18 |
| Distributed | 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 |
| Countries outside the US | AE, AR, AU, BE, BR, CA, CH, CN, DE, ES, GB, IN, IT, JO, JP, KR, MX, NZ, SA, SG, SV, TW |
| Quantity | 47,682 units |
| Reason classes | packaging |
| Model numbers | 00-1146-040, 045, 050, 055, 060, 065, 070, 075, 080, 085, 090, 095, 100-32 |
Product
Magna-Fx Cannulated Screw Fixation System Cannulated Bone Screw Sterile zimmer
Reason for recall
Zimmer is recalling various trauma screws that failed a leak test due to damage of the inner cavity only.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2245-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.