# FDA recall Z-2422-2023

> **Carefusion 2200 Inc** · Class II · device recall initiated 2023-07-13.

## Product

Snowden-Pencer MIS  DIAMOND-TOUCH CLAMP BOWEL 60 MM JAW 5MM, 32CM, RATCHETED, REF SP90-7046; endoscopic surgical device

## Reason for recall

Specific lots of the product have the potential to exhibit cracking or breaking of the rotation knob due to the incorrect use of an adhesive in the manufacturing process.

## Distribution

US and Canada

## Key facts

- **Recall number:** Z-2422-2023
- **Recalling firm:** Carefusion 2200 Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-07-13
- **Report date:** 2023-08-23

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Vernon Hills, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2422-2023

## Citation

> AI Analytics. FDA recall Z-2422-2023. Retrieved 2026-06-12 from https://api.ai-analytics.org/recall/Z-2422-2023. Source: US FDA. Licensed CC0.

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