Philips Healthcare DigitalDiagnost System X-Ray
FDA device recall Z-1554-2015 · posted 2015-05-19 · Terminated
Recall details
- Recalling firm
- Philips Medical Systems, Inc.
- Reason for recall
- The system is designed to emit a beep upon termination of an exposure. However, if the system has been powered on for over 12 hours, the system will no longer emit this signal. This is a failure to comply with 21CFR 1020.31(j).
- Action taken
- Philips Healthcare Planned action: 1. Philips healthcare will contact customers and initiate a software update to correct the software deficiency causing the problem. 2. Philips engineers will install the software. 3. Philips engineers will perform testing to ensure the software update was effective. 4. Corrections are to be made free of charge 5. Corrective actions should be completed by August 15, 2015 For further questions call (978) 659-7892
- Root cause
- Software design (manufacturing process)
- Status
- Terminated
- Product code
- MQB
- Quantity affected
- 54 DigitalDiagnost
- Distribution
- Worldwide Distribution - Nationwide Distribution and the countries of Australia, Austria, Argentina, Canada, China, Chile, Colombia Czech Republic, Great Britain, Germany, Egypt, Finland, France, Indi
- Date initiated
- 2015-02-09
- Date posted
- 2015-05-19
- Date terminated
- 2016-06-14
- Location
- Andover, MA
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Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| PHILIPS PROGRADE; PHILIPS ELEVA WORKSPOT FOR DIGITAL DIAGNOST (K141736) | Philips Medical Systems Dmc GmbH | 2014-07-25 |