# FDA recall Z-0144-2024

> **Covidien** · Class I · device recall initiated 2023-09-28.

## Product

Stolen McGRATH MAC Video Laryngoscopes, REF: 301-000-000

## Reason for recall

Defective video laryngoscopes that did not pass quality tests established for the product, that were designated for destruction, were stolen, and subsequently distributed for sale. Defective device use may result in failed laryngoscopy and/or intubation.

## Distribution

Unknown

## Key facts

- **Recall number:** Z-0144-2024
- **Recalling firm:** Covidien
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-09-28
- **Report date:** 2023-11-08

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Boulder, CO, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0144-2024

## Citation

> AI Analytics. FDA recall Z-0144-2024. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-0144-2024. Source: US FDA. Licensed CC0.

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