BrightView product code: 882478 BrightView X product code: 882480… — Class II medical device recall Z-0450-2015
Terminated recall by Philips Medical Systems (Cleveland) Inc, reported 2014-12-03, distributed in AR, CA, FL, GA, ID, LA, ME, MI…. Software issues
| Recall number | Z-0450-2015 |
|---|---|
| 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 | 2014-11-04 |
| Classified | 2014-11-25 |
| Reported by FDA | 2014-12-03 |
| Terminated | 2018-07-02 |
| Distributed | AR, CA, FL, GA, ID, LA, ME, MI, MN, MO, MS, NJ, NY, OH, OK, PA, TX |
| Countries outside the US | CA, CH, CN, DE, DK, ES, GB, IT, KR, SE, TW |
| Quantity | 85 |
| Reason classes | software |
Product
BrightView product code: 882478 BrightView X product code: 882480 BrightView XCT product code: 882482 and 882454
Reason for recall
Software issues
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-0450-2015. 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.