#1 MAC F/O LARYNGOSCOPE — Class II medical device recall Z-1288-2022
Terminated recall by Baxter Healthcare Corporation, reported 2022-07-06, distributed nationwide. Packaging error.
| Recall number | Z-1288-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Baxter Healthcare Corporation, Deerfield, IL, United States |
| Recall initiated | 2022-05-17 |
| Classified | 2022-06-24 |
| Reported by FDA | 2022-07-06 |
| Terminated | 2026-05-04 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AR, AT, AU, BD, BH, BO, BR, BS, CA, CL, CO, CR, CZ, DE, DO, EG, ES, FI, GT, GY, HN, ID, IN, IT, JP, KR, KW, MX, NL, NZ, PE, PH, PK, PL, SA, SV, TR, TT, UA, VN, ZA |
| Quantity | 99 units |
| UPC / GTIN / UDI-DI | 00732094141078, 00732094141382, 00732094230697 |
| Lot numbers | 21-056 |
Product
#1 MAC F/O LARYNGOSCOPE; F/O Laryngoscope Set-MAC; F/O Laryngoscope Set-MAC W/LED
Reason for recall
Packaging error.
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-1288-2022. 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.