MEERA CL mobile operating table — Class II medical device recall Z-0460-2025
Ongoing recall by Getinge Usa Sales Inc, reported 2024-11-20, distributed nationwide. Error code "50037" occurs on the IR-Hand Control when a MEERA-table is controlled, and the table stops the mov
| Recall number | Z-0460-2025 |
|---|---|
| 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 | 2024-10-03 |
| Classified | 2024-11-14 |
| Reported by FDA | 2024-11-20 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AT, AU, BR, CA, CH, CL, CO, CR, CZ, DE, EC, EG, ES, FR, GB, GR, HR, IL, IN, JO, JP, KR, KW, MX, MY, NL, NZ, PA, PE, PT, RO, RS, SA, SE, SG, SI, TH, TN, TR, UA, UY, VN, ZA |
| Quantity | 112 units |
| UPC / GTIN / UDI-DI | 04046768136298 |
| Model numbers | 710001B0 |
Product
MEERA CL mobile operating table - Designed for the placement and positioning of the patient immediately before, during and after surgical interventions, as well as for examination and treatment Item Number: 710001B0
Reason for recall
Error code "50037" occurs on the IR-Hand Control when a MEERA-table is controlled, and the table stops the movement. This error may occur sporadically when the MEERA-table is controlled via an IR-Hand Control and may result in procedural delay
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-0460-2025. 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.