Philips Healthcare Practix Convenio Mobile X-ray system recall
Philips Healthcare Practix Convenio Mobile X-ray system Worldwide Distribution -- Nationwide
Why was Philips Healthcare Practix Convenio Mobile X-ray system recalled?
When the system is switched off or when the tube arm is parked in the down position (X-ray generator switch off), a radiation pulse (50 kV, 2.5 pGy) is generated inadvertently. .When the system is switched off or when the tube arm is parked in the down position (X-ray generator switch off), a radiation pulse (50 kV, 2.5 pGy) is generated inadvertently. The failure happened when component supplie
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and identifiers are part of this recall.
- Product
- Philips Healthcare Practix Convenio Mobile X-ray system Worldwide Distribution -- Nationwide
- Recalling firm
- Philips Healthcare Inc.
- Quantity
- 11 - US
- Distribution
- Nationwide Distribution
- Recall date
- June 20, 2012
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)