Philips Xcelera Connect, Software R2.1 L 1 SP2, an interface engine for data exchange. Philips Xcelera Connect R2.x is a
FDA device recall Z-1942-2012 · posted 2012-07-05 · Terminated
Recall details
- Recalling firm
- Philips Healthcare Inc.
- Reason for recall
- Xcelera Connect R2.1 L 1 SP2 , incomplete information arriving from unformatted reports interface
- Action taken
- Philips Healthcare sent an "URGENT-FIELD SAFETY NOTICE" letter dated June 1, 2012 to all affected customers. The letter identifies the product, problem, and actions to be taken by the customers. A Philips representative will contact customers when the upgrade becomes available. Contact your local Philips Representative for questions concerning this issue.
- Root cause
- Software design
- Status
- Terminated
- Product code
- OUG
- Quantity affected
- 226 units
- Distribution
- Worldwide Distribution-USA (nationwide) and the countries of Argentina, Chile, Denmark , Estonia, Finland, France, Germany ,Hong Kong, Ireland, Italy, Malaysia, Netherlands, Poland, Saudi Arabia, Slov
- Date initiated
- 2012-06-14
- Date posted
- 2012-07-05
- Date terminated
- 2017-03-14
- Location
- Andover, MA
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