Philips Medical Systems (Cleveland) Inc Recall: Brilliance iCT and Brilliance iCT SP These
Philips Medical Systems (Cleveland) Inc Recall: Brilliance iCT and Brilliance iCT SP These is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Philips Medical Systems (Cleveland) Inc; Product: Brilliance iCT and Brilliance iCT SP These systems are intended to produce cross-sectional images
| Recalling firm | Philips Medical Systems (Cleveland) Inc |
|---|---|
| Product | Brilliance iCT and Brilliance iCT SP These systems are intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles and planes. May include signal analysis and display equipment, patient and equipment supports, components and accessories |
| Reason for recall | An artifact that resembles thrombus may appear on the image. |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Terminated |
| Distribution | Worldwide Distribution - USA (nationwide) including Puerto Rico and the states AL, AR, AZ, CA, DC, DE, FL, GA, IA, IL, IN, KY, MA, MD, MN, MO, MS, NC, NV, NY, OH, OK, OR, PA, SC, TX, VT, WA, and WV., and the countries of Argentina, Australia, Austria, Azerbaijan, Bangladesh, Belgium, Brazil, Chile, |
| Recall initiated | 20130716 |
| Recall number | Z-0831-2014 |
| Category | device |
| State | OH |
| Country | United States |
$29/mo
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