Covideien McGRATH MAC Video Laryngoscope — Class II medical device recall Z-2717-2024
Ongoing recall by Covidien, reported 2024-08-28, distributed nationwide. IFU update to address device's battery handling information.
| Recall number | Z-2717-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Covidien, Boulder, CO, United States |
| Recall initiated | 2024-07-09 |
| Classified | 2024-08-22 |
| Reported by FDA | 2024-08-28 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AR, AT, AU, BB, BD, BE, BG, BH, BM, BR, BS, CA, CH, CL, CN, CO, CR, CY, CZ, DE, DK, DZ, EE, EG, ES, FI, FR, GB, GH, GR, GT, GY, HK, HN, HR, HU, ID, IE, IL, IN, IQ, IR, IS, IT, JM, JO, JP, KE, KR, KW, KY, LB, LT, LU, LV, MA, MT, MX, MY, NG, NI, NL, NO, NP, NZ, OM, PA, PE, PH, PK, PL, PT, QA, RO, RS, SA, SE, SG, SI, SK, SV, TH, TN, TR, TT, TW, UA, UY, VN, ZA |
| Quantity | 68,093 devices |
| UPC / GTIN / UDI-DI | 10884521776494, 10884521823396 |
| Lot numbers | 000082, 000100, 000101, 000106, 000109, 000113, 000114, 000118, 000134, 000137, 000142, 000145, 000147, 000158, 000169, 000177, 000204, 000206, 000214, 000215, 000220, 000236, 000240, 000242, 000245, 000246, 000257, 000266, 000268, 000272, 000280, 000290, 000294, 000295, 000298, 000301, 000302, 000304, 000311, 000313 and 460 more |
| Model numbers | 301-000-000 |
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.
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-2717-2024. 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.