Data Foundry

Medical device recalls 2016

Implant EP Pick-Up Coping Dental implants — Class II medical device recall Z-2470-2016

Terminated recall by Biomet 3i, LLC, reported 2016-08-24, distributed nationwide. Pouches may not have been sealed during packing.

Recall numberZ-2470-2016
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmBiomet 3i, LLC, Palm Beach Gardens, FL, United States
Recall initiated2015-11-25
Classified2016-08-16
Reported by FDA2016-08-24
Terminated2019-07-26
DistributedNationwide (US)
Countries outside the USAE, 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 numbersIIC60, IIC75, WIP55, WIP56, WIP57, WIP66, WIP67

Product

Implant EP Pick-Up 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-2470-2016. 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.