# FDA recall Z-0105-2022

> **Centese Inc.** · Class II · device recall initiated 2021-08-31.

## Product

Thoraguard Chest Tube Kit, 20 Fr

## Reason for recall

An adhesive joint in the SmartValve component of the device can become compromised resulting in a leak.

## Distribution

Distribution to a single consignee located in California.

## Key facts

- **Recall number:** Z-0105-2022
- **Recalling firm:** Centese Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2021-08-31
- **Report date:** 2021-10-20
- **Termination date:** 2023-08-07

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Omaha, NE, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0105-2022

## Citation

> AI Analytics. FDA recall Z-0105-2022. Retrieved 2026-06-03 from https://api.ai-analytics.org/recall/Z-0105-2022. Source: US FDA. Licensed CC0.

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