# FDA recall Z-2636-2024

> **Covidien** · Class I · device recall initiated 2024-07-09.

## Product

McGrath Mac Video Laryngoscope, REF: 300-000-000 , Non-Sterile, Rx Only

## Reason for recall

Battery management system within Laryngoscope devices may deplete below the deign threshold which may result in thermal event followed by risk of explosion.

## Distribution

Worldwide - US Nationwide distribution including in the states of AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, 	NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY, Puerto Rico, Virgin Islands and the countries of Albania, Algeria, Andorra, Angola, Argentina, 	Australia, Austria, Azerbaijan, Bahamas, Bahrain, Bangladesh, Barbados, Belgium, Bermuda, Bhutan, Bosnia, Herzegovina, Botswana, Brazil, Bulgaria, Cambodia, Cameroon, 	Canada, Canary Islands, Cayman Islands, Chile, China, Colombia, Costa Rica, Croatia, 	Cyprus, Czech Republic, Denmark, Dominican, Rep.	Dutch Antilles, Egypt, El Salvador, 	Estonia, Faroe Islands, Fiji, Finland, France, French Guiana, French Polynesia, Germany, 	Ghana, Greece, Guadeloupe, Guatemala, Guyana, Honduras, Hong Kong, Hungary, Iceland, 	India, Indonesia, Iran, Islamic, Republic of Iraq, Ireland, Israel, Italy, Jamaica, Japan, Jordan, Kazakhstan, Ke

## Key facts

- **Recall number:** Z-2636-2024
- **Recalling firm:** Covidien
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-07-09
- **Report date:** 2024-08-28

- **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-2636-2024

## Citation

> AI Analytics. FDA recall Z-2636-2024. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-2636-2024. Source: US FDA. Licensed CC0.

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