GETINGE MEERA MOBILE OPERATING TABLE: — Class II medical device recall Z-1734-2019
Terminated recall by Maquet Cardiovascular Us Sales, Llc, reported 2019-06-12, distributed nationwide. User may suffer an electric shock when coming in contact with the exposed electronic components
| Recall number | Z-1734-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Maquet Cardiovascular Us Sales, Llc, Wayne, NJ, United States |
| Recall initiated | 2019-05-06 |
| Classified | 2019-06-04 |
| Reported by FDA | 2019-06-12 |
| Terminated | 2022-07-06 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AR, AT, AU, BD, BE, BG, BH, BO, BR, CA, CH, CL, CN, CO, CR, CZ, DE, DK, DZ, EC, EG, ES, FI, FR, GB, GR, HK, HN, HR, HU, IE, IL, IN, IR, IS, IT, JO, JP, KR, KW, LB, LT, LV, MA, MX, MY, NL, NO, NZ, PE, PH, PK, PL, PT, PY, RO, RS, SA, SE, SG, SI, SK, TH, TR, TW, UA, UY, VN, ZA |
| Lot numbers | 119, 1417, 1689, 221, 226, 417, 503, 701, 710001B0, 710001B2, 711, 720001B0, 720001B2, 720001F0, 720001F2 |
| Model numbers | 1416, 220, 416, 710001B0, 710001B2, 710001F0, 720001B0, 720001B2, 720001F0, 720001F2 |
Product
GETINGE MEERA MOBILE OPERATING TABLE: (1) Part 720001B2 (2) Part 720001B0 (3) Part 720001F2 (4) Part 720001F0 (5) Part 710001B2 (6) Part 710001B0 (7) Part 710001F0 Product Usage: The Meera Mobile Operating Table is designed to support and position the patient immediately before, during and after surgical interventions as well as for examination and treatment.
Reason for recall
User may suffer an electric shock when coming in contact with the exposed electronic components
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-1734-2019. 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.