Data Foundry

Medical device recalls 2022

BASIN SET — Class II medical device recall Z-0274-2023

Terminated recall by American Contract Systems, Inc., reported 2022-11-30, distributed nationwide. Basin Set labeling error: components within the kit are for the Single Basin Set. Therefore, the contents of t

Recall numberZ-0274-2023
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmAmerican Contract Systems, Inc., Kansas City, MO, United States
Recall initiated2022-10-12
Classified2022-11-22
Reported by FDA2022-11-30
Terminated2025-03-06
DistributedNationwide (US)
Quantity1,504 trays
Reason classeslabeling
UPC / GTIN / UDI-DI00191072151742
Lot numbers833221
Expiration dates2023-06-16

Product

BASIN SET, MEBS42K, general surgical kit

Reason for recall

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.

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-0274-2023. 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.