FDA Device recall Z-0274-2023
BASIN SET, MEBS42K, general surgical kit
- FDA Device
- Class II
- terminated
- Published 2022-11-30
On 2022-11-30 the FDA classified a Class II recall of BASIN SET, MEBS42K, general surgical kit by American Contract Systems, citing basin Set labeling error: components within the kit are for the Single Basin Set. Therefore, the contents of the package do not match the contents listed on the label.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0274-2023 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2022-10-12 |
| Published | 2022-11-30 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | American Contract Systems |
| Distribution | US |
Product
BASIN SET, MEBS42K, general surgical kit
Reason
Basin Set labeling error: components within the kit are for the Single Basin Set. Therefore, the contents of the package do not match the contents listed on the label.
Identifiers
| code_info | UDI/DI 00191072151742, Batch/Lot No. 833221, exp 6/16/2023 |
|---|
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-0274-2023%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.