BrightView XCT: product code 882482 — Class II medical device recall Z-1982-2014
Terminated recall by Philips Medical Systems (Cleveland) Inc, reported 2014-07-09, distributed in AZ, CA, CO, DC, FL, GA, HI, IA…. Flat Panel Display (FPD) failed to remain securely locked in the deployed position.
| Recall number | Z-1982-2014 |
|---|---|
| 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 | 2014-06-23 |
| Classified | 2014-07-02 |
| Reported by FDA | 2014-07-09 |
| Terminated | 2015-09-24 |
| Distributed | AZ, CA, CO, DC, FL, GA, HI, IA, IL, KY, MA, MD, MN, MO, MS, MT, NC, ND, NE, NJ, NV, NY, OH, OK, OR, PA, SD, TX, VT, WA, WI, WV |
| Countries outside the US | AE, AR, AT, AU, BE, BR, CA, CH, CL, CN, CZ, DE, DK, DZ, ES, FI, FR, GB, GR, ID, IE, IL, IT, JP, KR, LB, MX, MY, NL, NO, NZ, PA, PL, PT, RU, SA, SE, SK, TR, TW, ZA |
| Quantity | 407 |
Product
BrightView XCT: product code 882482, BrightView X- upgraded with the XCT Flat Panel Detector (FPD): product code 882454. Gamma camera for Single Photon Emission Computed Tomography (SPECT) Medical Device for imaging.
Reason for recall
Flat Panel Display (FPD) failed to remain securely locked in the deployed position.
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-1982-2014. 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.