Philips Xcelera Connect recall
Philips Xcelera Connect, Software R2.1 L 1 SP2, an interface engine for data exchange. Philips Xcelera Connect R2.x is a generic interface and data…
Why was Philips Xcelera Connect recalled?
Xcelera Connect R2.1 L 1 SP2 , incomplete information arriving from unformatted reports interface
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 lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Software R2.1 L 1 SP2
- Product
- Philips Xcelera Connect, Software R2.1 L 1 SP2, an interface engine for data exchange. Philips Xcelera Connect R2.x is a generic interface and data…
- Recalling firm
- Philips Healthcare Inc.
- Quantity
- 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, Slovenia, South Africa, Spain, Sweden, Taiwan, United Kingdom, and Utd. Arab. Emir.
- Recall date
- July 11, 2012
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)