FDA Device recall Z-1501-2022
Turbett Surgical Container, TS1500
- FDA Device
- Class II
- terminated
- Published 2022-08-10
On 2022-08-10 the FDA classified a Class II recall of Turbett Surgical Container, TS1500 by Turbett Surgical, citing devices were subject to unapproved rework processes.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1501-2022 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2022-04-14 |
| Published | 2022-08-10 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Turbett Surgical |
| Distribution | US |
Product
Turbett Surgical Container, TS1500
Reason
Devices were subject to unapproved rework processes.
Identifiers
| code_info | UDI-DI (GTIN): 00859464007113; Lot No./Serial No.: 100036/2017061015, 100036/2017061016, 100036/2017061017, 100036/2017…UDI-DI (GTIN): 00859464007113; Lot No./Serial No.: 100036/2017061015, 100036/2017061016, 100036/2017061017, 100036/2017061019, 100036/2017061023, 100036/2017061025, 100065/2017121001 and 100081/2018031004. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1501-2022%22
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