FDA Device recall Z-1288-2022
#1 MAC F/O LARYNGOSCOPE
- FDA Device
- Class II
- terminated
- Published 2022-07-06
On 2022-07-06 the FDA classified a Class II recall of #1 MAC F/O LARYNGOSCOPE by Baxter Healthcare, citing packaging error.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1288-2022 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2022-05-17 |
| Published | 2022-07-06 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Baxter Healthcare |
| Distribution | US |
Product
#1 MAC F/O LARYNGOSCOPE; F/O Laryngoscope Set-MAC; F/O Laryngoscope Set-MAC W/LED
Reason
Packaging error.
Identifiers
| code_info | Product Codes: 69061 (UDI/DI:732094141382), 69696 (UDI/DI: 732094141078), 69696-LED (UDI/DI: 732094230697); Lot code: 21-056 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1288-2022%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.