MR Surgical Suite II Table — Class II medical device recall Z-0196-2016
Terminated recall by GE Medical Systems, LLC, reported 2015-11-11, distributed in AZ, CA, CO, FL, IL, MI, MN, OH…. GE became aware of an issue with the table transfer release mechanism of the MR Surgical Suite Option. The iss
| Recall number | Z-0196-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | GE Medical Systems, LLC, Waukesha, WI, United States |
| Recall initiated | 2015-09-23 |
| Classified | 2015-10-30 |
| Reported by FDA | 2015-11-11 |
| Terminated | 2016-03-28 |
| Distributed | AZ, CA, CO, FL, IL, MI, MN, OH, TX, WI |
| Countries outside the US | AT, BR, CA, CN, CZ, DE, FR, GB, JP, PL, TR, ZA |
| Model numbers | M0001SS, M0074SS, M8053SS, M8074SS |
Product
MR Surgical Suite II Table, Model Number(s): M8074SS, M8053SS, M0074SS. UPDATE 11-4-2015: Model M0001SS
Reason for recall
GE became aware of an issue with the table transfer release mechanism of the MR Surgical Suite Option. The issue may prevent patient transfer between the MR and surgical tables.
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-0196-2016. 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.