FDA Device recall Z-3207-2017
TRY-IN,ABUTMENT, CONT, 3.5X4.5, REF ZOAT34
- FDA Device
- Class II
- terminated
- Published 2017-10-04
On 2017-10-04 the FDA classified a Class II recall of TRY-IN,ABUTMENT, CONT, 3.5X4.5, REF ZOAT34 by Zimmer Dental, citing zimmer Biomet is conducting a medical device field correction for various dental products due to several parts being shipped to the customer with only standard IFUs. All the produ….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-3207-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-07-10 |
| Published | 2017-10-04 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Zimmer Dental |
| Distribution | n/a |
Product
TRY-IN,ABUTMENT, CONT, 3.5X4.5, REF ZOAT34; TRY-IN, ABUTMENT, CONT, 4.5X5.5, REF ZOAT45; TRY-IN, ABUTMENT, CONT, 5.7X6.5, REF ZOAT56; TRY-IN KIT, ABUTMENT, CONT, REF ZOATKIT
Reason
Zimmer Biomet is conducting a medical device field correction for various dental products due to several parts being shipped to the customer with only standard IFUs. All the products were missing supplemental IFUs.
Identifiers
| code_info | lot # 63145351, 63202941, 60646055, 62353334, 63316134 |
|---|
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-3207-2017%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.