FEM IM NAIL 15MMDX30CM — Class II medical device recall Z-2596-2017
Terminated recall by Zimmer Biomet, Inc., reported 2017-06-21, distributed in AK, AL, AR, AZ, CA, CO, CT, FL…. Zimmer Biomet is initiating a field action for sterile-packaged implants packaged in a single package configur
| Recall number | Z-2596-2017 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Zimmer Biomet, Inc., Warsaw, IN, United States |
| Recall initiated | 2017-04-28 |
| Classified | 2017-06-15 |
| Reported by FDA | 2017-06-21 |
| Terminated | 2019-05-15 |
| Distributed | AK, AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY |
| Countries outside the US | AE, AR, AU, BE, BR, CA, CH, CN, DE, DZ, EG, ES, FR, GB, GT, HN, IN, IT, JM, JO, JP, KR, LB, MA, MX, MY, NI, NL, NZ, PA, PE, PL, SA, SG, SV, TH, TW |
| Quantity | 27,279 |
| Reason classes | sterility |
| Lot numbers | 367348, 367352, 367354, 367355, 367355R, 367737, 367737R, 367739, 367739R, 367749, 367749R, 367750, 367750R, 367751, 367752, 367753, 367753R, 367766, 367766R, 367767, 367779, 367781, 367877, 367878, 367878R, 367881, 367882, 367882R, 367983, 367984, 367985, 367985R, 367986, 367986R, 368032, 368033, 368034, 368041, 368042, 368069 and 460 more |
| Model numbers | 00225230015, 00225230016, 00225232014, 00225232015, 00225232016, 00225234014, 00225234015, 00225234016, 00225236014, 00225236015, 00225238014, 00225238015, 00225240011, 00225240013, 00225240014, 00225240015, 00225242011, 00225242012, 00225242013, 00225242014, 00225242015, 00225244011, 00225244012, 00225244013, 00225244014 and 12 more |
Product
FEM IM NAIL 15MMDX30CM, FEM IM NAIL 16MMDX30CM FEM IM NAIL 14MMDX32CM FEM IM NAIL 15MMDX32CM FEM IM NAIL 16MMDX32CM FEM IM NAIL 14MMDX34CM FEM IM NAIL 15MMDX34CM FEM IM NAIL 16MMDX34CM FEM IM NAIL 14MMDX36CM FEM IM NAIL 15MMDX36CM FEM IM NAIL 14MMDX38CM FEM IM NAIL 15MMDX38CM FEM IM NAIL 11MMDX40CM FEM IM NAIL 13MMDX40CM FEM IM NAIL 14MMDX40CM FEM IM NAIL 15MMDX40CM FEM IM NAIL 11MMDX42CM FEM IM NAIL 12MMDX42CM FEM IM NAIL 13MMDX42CM FEM IM NAIL 14MMDX42CM FEM IM NAIL 15MMDX42CM FEM IM NAIL 11MMDX44CM FEM IM NAIL 12MMDX44CM FEM IM NAIL 13MMDX44CM FEM IM NAIL 14MMDX44CM FEM IM NAIL 10MMDX46CM FEM IM NAIL 11MMDX46CM FEM IM NAIL 12MMDX46CM FEM IM NAIL 13MMDX46CM FEM IM NAIL 14MMDX46CM FEM IM NAIL 10MMDX48CM FEM IM NAIL 11MMDX48CM FEM IM NAIL 12MMDX48CM FEM IM NAIL 13MMDX48CM FEM IM NAIL 14MMDX48CM FEM IM NAIL 13MMDX50CM FEM IM NAIL 14MMDX50CM
Reason for recall
Zimmer Biomet is initiating a field action for sterile-packaged implants packaged in a single package configuration due to packaging design verification test failures.
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-2596-2017. 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.