Brilliance CT 6 — Class II medical device recall Z-2210-2013
Terminated recall by Philips Medical Systems (Cleveland) Inc, reported 2013-09-25, distributed nationwide. The patient support may move in an unintended manner if the footswitch cover impinges on the footswitch.
| Recall number | Z-2210-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Philips Medical Systems (Cleveland) Inc, Cleveland, OH, United States |
| Recall initiated | 2013-07-05 |
| Classified | 2013-09-16 |
| Reported by FDA | 2013-09-25 |
| Terminated | 2015-09-15 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AT, AU, CH, CL, CN, DE, DK, FR, GB, HR, ID, IL, IS, JP, KR, NG, NL, NO, PL, RO, SE, TW, VN, ZA |
| Serial numbers | 10009, 10011, 10012, 10015, 10028, 10036, 10042, 10045, 10050, 10052, 10062, 10063, 10064, 10077, 10079, 10081, 10096, 10099, 10102, 10111, 10114, 10120, 10122, 10135, 10136 and 284 more |
| Model numbers | 728231, 728235, 728246, 728256 |
Product
Brilliance CT 6, M/N 728256; Brilliance CT 16 M/N 728246; Brilliance CT 40, M/N 728235 & Brilliance CT 64 M/N 728231, Philips Healthcare, Cleveland, OH 44143. Intended to produce cross-sectional images of the body by computer reconstruction.
Reason for recall
The patient support may move in an unintended manner if the footswitch cover impinges on the footswitch.
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-2210-2013. 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.