Data Foundry

Medical device recalls 2024

McGRATH" MAC EMS Video Laryngoscope — Class I medical device recall Z-2637-2024

Ongoing recall by Covidien, reported 2024-08-28, distributed nationwide. Battery management system within Laryngoscope devices may deplete below the deign threshold which may result i

Recall numberZ-2637-2024
Product typeMedical device
ClassificationClass I
StatusOngoing
Voluntary or mandatedVoluntary
Recalling firmCovidien, Boulder, CO, United States
Recall initiated2024-07-09
Classified2024-08-21
Reported by FDA2024-08-28
DistributedNationwide (US)
Countries outside the USAE, 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
Quantity10,449 units
UPC / GTIN / UDI-DI15060272980112
Serial numbers366170, 366176, 366180, 366187, 366189, 366194, 366200, 366205, 366208, 366210, 366212, 366214, 366215, 366230, 366232, 366234, 366235, 366238, 366241, 366243, 366244, 366246, 366247, 366250, 366252 and 475 more
Model numbers300-200-000

Product

McGRATH" MAC EMS Video Laryngoscope, REF: 300-200-000 , Non-Sterile, Rx Only

Reason for recall

Battery management system within Laryngoscope devices may deplete below the deign threshold which may result in thermal event followed by risk of explosion.

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-2637-2024. 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.