Stolen McGRATH MAC Video Laryngoscopes — Class I medical device recall Z-0144-2024
Ongoing recall by Covidien, reported 2023-11-08. Defective video laryngoscopes that did not pass quality tests established for the product, that were designate
| Recall number | Z-0144-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class I |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Covidien, Boulder, CO, United States |
| Recall initiated | 2023-09-28 |
| Classified | 2023-11-02 |
| Reported by FDA | 2023-11-08 |
| Quantity | 5,709 |
| UPC / GTIN / UDI-DI | 10884521776494, 20884521823393 |
| Serial numbers | 000063, 000076, 000085, 000092, 000093, 000112, 000120, 000121, 000146, 000153, 000154, 000155, 000166, 000179, 000190, 000197, 000202, 000224, 000233, 000238, 000255, 000308, 000329, 000375, 000389 and 475 more |
| Model numbers | 301-000-000 |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0144-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.