Philips DXR System, DuraDiagnost Rel. 4. Stationary X-Ray System.
Reported: April 23, 2025 Initiated: March 10, 2025 #Z-1554-2025
Product Description
Philips DXR System, DuraDiagnost Rel. 4. Stationary X-Ray System.
Reason for Recall
Potential for collimator to fall as a result of incorrect installation.
Details
- Recalling Firm
- Philips North America Llc
- Units Affected
- 83 units
- Distribution
- Worldwide - US Nationwide distribution in the states of AK, FL, KS, MS, NH, NY, OR, PA, TX, WI and the countries of Argentina, Australia, Canada, Chile, China, Germany, Hungary, India, Indonesia, Italy, Kenya, Mexico, Netherlands, New Zealand, Oman, Pakistan, Peru, Poland, Romania, Russian Federation, Slovenia, South Africa, Spain, Thailand, United Kingdom, Vietnam.
- Location
- Cambridge, MA
Frequently Asked Questions
What product was recalled? ▼
Philips DXR System, DuraDiagnost Rel. 4. Stationary X-Ray System.. Recalled by Philips North America Llc. Units affected: 83 units.
Why was this product recalled? ▼
Potential for collimator to fall as a result of incorrect installation.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on April 23, 2025. Severity: Moderate. Recall number: Z-1554-2025.
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