Maquet Getinge Group 1180 — Class II medical device recall Z-1045-2016
Terminated recall by Maquet Cardiovascular Us Sales, Llc, reported 2016-03-09, distributed in AZ, MO. MAQUET Medical Systems USA is initiating a field action for correction of the MAQUET Extension Device (Part No
| Recall number | Z-1045-2016 |
|---|---|
| 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 | 2016-01-07 |
| Classified | 2016-03-03 |
| Reported by FDA | 2016-03-09 |
| Terminated | 2017-05-25 |
| Distributed | AZ, MO |
| Countries outside the US | AE, AT, AU, BE, BH, BR, CA, CH, DE, DK, EC, EE, ES, FI, FR, GB, HK, IN, IT, JP, KR, LV, MY, NL, NO, PL, PT, RS, RU, SA, SE, TW, VE |
| Serial numbers | 00003, 00004 |
| Model numbers | 1180.19F0 |
Product
Maquet Getinge Group 1180.19XO Extension Device. Manufacturer MAQUET GmbH, Used to support the upper and lower extremities immediately before, during and after fracture surgery. The Extension Device (1180.19F0) is a table top module for use with the Maquet MAGNUS operating table system and it is attached to the base mounting point of the MAGNUS operating table.
Reason for recall
MAQUET Medical Systems USA is initiating a field action for correction of the MAQUET Extension Device (Part No 1180.19F0). The Extension Device is manufactured by Maquet GmbH, in Germany, and is a table top module for use with the Maquet MAGNUS operating table system. Maquet GmbH was made aware of a potential issue that can result in the Extension Device becoming unlocked from the table top, causing it to fall down.
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-1045-2016. 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.