Philips DigitalDiagnost 3.1.x X-Ray System
Reported: June 21, 2017 Initiated: May 11, 2017 #Z-2154-2017
Product Description
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.
Details
- Recalling Firm
- Philips Electronics North America Corporation
- Units Affected
- US - 132
- 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
- Location
- Andover, MA
Frequently Asked Questions
What product was recalled? ▼
Philips DigitalDiagnost 3.1.x X-Ray System. Recalled by Philips Electronics North America Corporation. Units affected: US - 132.
Why was this product recalled? ▼
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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on June 21, 2017. Severity: Moderate. Recall number: Z-2154-2017.
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