# FDA recall Z-0955-2023

> **Covidien, LLC** · Class II · device recall initiated 2022-11-23.

## Product

COVIDIEN Emprint Ablation Catheter with Thermosphere Technology, Bronchoscopic Ablation, REF CA108L1

## Reason for recall

The product is labeled with the incorrect expiration date.

## Distribution

Foreign Distribution: Hong Kong

## Key facts

- **Recall number:** Z-0955-2023
- **Recalling firm:** Covidien, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-11-23
- **Report date:** 2023-01-18

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Minneapolis, MN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0955-2023

## Citation

> AI Analytics. FDA recall Z-0955-2023. Retrieved 2026-08-12 from https://api.ai-analytics.org/recall/Z-0955-2023. Source: US FDA. Licensed CC0.

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