Recall Z-0144-2024— Covidien
Class I · Ongoing
Class I FDA medical device recall by Covidien, initiated 2023-09-28. FDA's recall record names no specific 510(k) clearance for this event. Product: Stolen McGRATH MAC Video Laryngoscopes, REF: 301-000-000. Reason: 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..
- Recalling firm
- Covidien
- Classification
- Class I
- Status
- Ongoing
- Initiated
- 2023-09-28
- Firm location
- Boulder, CO, United States
Product description
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.