# FDA recall Z-0274-2023

> **American Contract Systems, Inc.** · Class II · device recall initiated 2022-10-12.

## 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.

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-0274-2023
- **Recalling firm:** American Contract Systems, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2022-10-12
- **Report date:** 2022-11-30
- **Termination date:** 2025-03-06

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Kansas City, MO, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0274-2023

## Citation

> AI Analytics. FDA recall Z-0274-2023. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-0274-2023. Source: US FDA. Licensed CC0.

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