Philips Electronics North America Corporation Recall: Philips DigitalDiagnost 3.1.x X-Ray
Philips Electronics North America Corporation Recall: Philips DigitalDiagnost 3.1.x X-Ray is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Philips Electronics North America Corporation; Product: Philips DigitalDiagnost 3.1.x X-Ray System; Reason for recall: During recent evaluations of
| Recalling firm | Philips Electronics North America Corporation |
|---|---|
| Product | Philips DigitalDiagnost 3.1.x X-Ray System |
| Reason for recall | During recent evaluations of the Philips DigitalDiagnost 3.1.x, we have identified a potential issue that may affect the performance of the equipment under certain conditions. |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Terminated |
| Distribution | USA(nationwide) Distribution to the states of : AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, IL, IN, KY, LA, MA, ME, MI, MN, MO, NC, ND, NE, NH, NM, NY, OH, OK, OR, PA, TN, TX, UT, VA, WA and WI |
| Recall initiated | 20170511 |
| Recall number | Z-2154-2017 |
| Category | device |
| State | MA |
| Country | United States |
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