Locator Abutment Impression Coping Dental implants — Class II medical device recall Z-2481-2016
Terminated recall by Biomet 3i, LLC, reported 2016-08-24, distributed nationwide. Pouches may not have been sealed during packing.
| Recall number | Z-2481-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Biomet 3i, LLC, Palm Beach Gardens, FL, United States |
| Recall initiated | 2015-11-25 |
| Classified | 2016-08-16 |
| Reported by FDA | 2016-08-24 |
| Terminated | 2019-07-26 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AR, AT, AU, BB, BE, BO, BR, CA, CH, CL, CN, CO, CR, DE, DK, DO, ES, FR, GB, GR, HK, HU, IE, IL, IN, IT, JM, JP, KR, KW, KY, LB, LT, MX, NL, PE, PL, PT, PY, QA, SA, SE, SG, SI, TH, TR, TT, TW, UY, VN, ZA |
| Model numbers | LAIC1 |
Product
Locator Abutment Impression Coping Dental implants
Reason for recall
Pouches may not have been sealed during packing.
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-2481-2016. 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.