RePlant¿ Angled Abutment Part Number 6050-52-60 — Class II medical device recall Z-2320-2016
Terminated recall by Implant Direct Sybron Manufacturing, LLC, reported 2016-08-10, distributed in AL, AR, AZ, CA, DE, FL, GA, KS…. Issue with design specification; oversized condition.
| Recall number | Z-2320-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Implant Direct Sybron Manufacturing, LLC, Westlake Village, CA, United States |
| Recall initiated | 2016-07-05 |
| Classified | 2016-08-02 |
| Reported by FDA | 2016-08-10 |
| Terminated | 2017-02-16 |
| Distributed | AL, AR, AZ, CA, DE, FL, GA, KS, LA, MA, MI, MO, NC, NE, NY, OK, OR, SC, TN, TX, UT, VA, WA, WI |
| Quantity | 205 |
| Lot numbers | 39799, 49364, 50174 |
| Model numbers | 6050-52-60 |
Product
RePlant¿ Angled Abutment Part Number 6050-52-60
Reason for recall
Issue with design specification; oversized condition.
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-2320-2016. 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.