Recall Z-2717-2024— Covidien
Class II · Ongoing
Class II FDA medical device recall by Covidien, initiated 2024-07-09. FDA's recall record names no specific 510(k) clearance for this event. Product: Covideien McGRATH MAC Video Laryngoscope, REF: 301-000-000, Non-Sterile, RxOnly. Reason: IFU update to address device's battery handling information..
- Recalling firm
- Covidien
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2024-07-09
- Firm location
- Boulder, CO, United States
Product description
Covideien McGRATH MAC Video Laryngoscope, REF: 301-000-000, Non-Sterile, RxOnly
Reason for recall
IFU update to address device's battery handling information.
Data sourced from openFDA. This site is unofficial and independent of the FDA.