ALPHAMAXX Mobile Operating Table — Class II medical device recall Z-2273-2024
Ongoing recall by Getinge Usa Sales Inc, reported 2024-07-17, distributed in KY, NC, NY, VA. The recall is prompted by a defective charger unit (0970.2873) for models 1133.22B4, 1133.22B5, and 1133.22F5
| Recall number | Z-2273-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Getinge Usa Sales Inc, Wayne, NJ, United States |
| Recall initiated | 2024-05-29 |
| Classified | 2024-07-05 |
| Reported by FDA | 2024-07-17 |
| Distributed | KY, NC, NY, VA |
| Countries outside the US | AE, AU, BG, CH, CZ, DK, ES, FR, GB, GR, HK, HR, IE, IL, JO, JP, KW, MX, NO, NZ, PL, RO, SA, TH, ZA |
| Quantity | 7 units |
| UPC / GTIN / UDI-DI | 04046768040052 |
| Serial numbers | 409 |
| Model numbers | 113322F5 |
Product
ALPHAMAXX Mobile Operating Table, Model Number/Part Number: 113322F5
Reason for recall
The recall is prompted by a defective charger unit (0970.2873) for models 1133.22B4, 1133.22B5, and 1133.22F5 of the ALPHAMAXX mobile operating table. This issue poses a risk of inadequate charging and operational failure.
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-2273-2024. 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.