BrightView SPECT model number 882480 BrightView and BrightView X are… — Class II medical device recall Z-1750-2017
Terminated recall by Philips Medical Systems (Cleveland) Inc, reported 2017-04-12, distributed in AR, AZ, CA, CO, CT, FL, GA, IA…. The brake hub was not engaging with the gear box shaft due to an error in the assembly of components within th
| Recall number | Z-1750-2017 |
|---|---|
| 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 | 2017-02-24 |
| Classified | 2017-04-06 |
| Reported by FDA | 2017-04-12 |
| Terminated | 2018-07-02 |
| Distributed | AR, AZ, CA, CO, CT, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, NC, NJ, NY, OH, OR, PA, SD, TN, TX, VA, WA, WI, WV |
| Countries outside the US | AE, AT, AU, BE, BR, CA, CH, CL, CN, DE, DK, EG, ES, FR, GB, IL, IN, IT, JP, KR, MX, MY, NL, PH, PL, PT, SA, TW, ZA |
| Quantity | 84 systems |
| Model numbers | 882480 |
Product
BrightView SPECT model number 882480 BrightView and BrightView X are gamma cameras designed for single or dual detector nuclear imaging accommodating a broad range of Emission Computed Tomography (ECT) studies. The cameras can be used to perform planar static, dynamic, gated, and total body studies, as well as circular-orbit and noncircular orbit SPECT studies, gated SPECT (circular and noncircular)studies, computer-programmed protocol strings, and reference scans (dual detectors only).
Reason for recall
The brake hub was not engaging with the gear box shaft due to an error in the assembly of components within the brake hub mechanism after service, causing the detector to backdrive.
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-1750-2017. 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.