FDA Device recall Z-2320-2016
RePlant¿ Angled Abutment Part Number 6050-52-60
- FDA Device
- Class II
- terminated
- Published 2016-08-10
On 2016-08-10 the FDA classified a Class II recall of RePlant¿ Angled Abutment Part Number 6050-52-60 by Implant Direct Sybron Manufacturing, citing issue with design specification; oversized condition.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2320-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-07-05 |
| Published | 2016-08-10 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Implant Direct Sybron Manufacturing |
| Distribution | AL, AR, AZ, CA, DE, FL, GA, KS, LA, MA, MI, MO, NC, NE, NY, OK, OR, SC, TN, TX, UT, VA, WA, WI |
Product
RePlant¿ Angled Abutment Part Number 6050-52-60
Reason
Issue with design specification; oversized condition.
Identifiers
| code_info | Lot #50174, 39799, 49364 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2320-2016%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.