McGrath Mac 2 — Class II medical device recall Z-0169-2024
Ongoing recall by Covidien, reported 2023-11-08, distributed in AK, AL, AR, AZ, CA, CO, CT, DE…. Laryngoscope blades may contain an ineffective application of anti-fog agent which may result in condensation
| Recall number | Z-0169-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Covidien, Boulder, CO, United States |
| Recall initiated | 2023-08-10 |
| Classified | 2023-11-01 |
| Reported by FDA | 2023-11-08 |
| Distributed | AK, AL, AR, AZ, CA, CO, CT, DE, FL, GA, IA, IL, IN, KS, LA, MA, MD, MI, MO, MT, NC, ND, NH, NJ, NM, NY, OH, OK, OR, PA, SD, TN, TX, UT, VA, WA, WI, WY |
| Countries outside the US | AE, AT, AU, BE, BS, CH, CZ, DE, DK, ES, FI, FR, HK, HR, HU, IE, IL, IT, KR, MT, NL, NO, NZ, PK, PL, PT, RO, SE |
| Quantity | 42,367 |
| UPC / GTIN / UDI-DI | 10884521824386 |
| Lot numbers | 22102001 |
| Model numbers | 350-084-000 |
Product
McGrath Mac 2, Disposable Laryngoscope Blade, REF: 350-084-000, Sterile EO, Rx Only
Reason for recall
Laryngoscope blades may contain an ineffective application of anti-fog agent which may result in condensation accumulating causing the screen to be blurred or obscured.
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-0169-2024. 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.