# FDA recall Z-2717-2024

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

## Product

Covideien McGRATH MAC Video Laryngoscope, REF: 301-000-000, Non-Sterile, RxOnly

## Reason for recall

IFU update to address device's battery handling information.

## 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, US Virgin Islands and the countries of Albania, Algeria, Andorra, Angola, 	Argentina, Australia, Austria, Azerbaijan, Bahamas, Bahrain, Bangladesh, Barbados, 	Belgium, Bermuda, Bhutan, Bosnia And 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, Kazakh

## Key facts

- **Recall number:** Z-2717-2024
- **Recalling firm:** Covidien
- **Classification:** Class II
- **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-2717-2024

## Citation

> AI Analytics. FDA recall Z-2717-2024. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-2717-2024. Source: US FDA. Licensed CC0.

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