Capnostream 20p recall
CAPNOSTREAM 20P (COV-INTL) N W/PRINTER ROHS, CS051COV
Why was Capnostream 20p recalled?
The date/time, nurse call and alarm settings of the bedside patient monitors may reset to the factory default settings when the monitor is powered off.
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?
ME30160001 ME30160002 ME30160003 ME30160004 ME30160005 ME30160006 ME30160007 ME30160008 ME30160009 ME30160010 ME30160011 ME30160012 ME30160013 ME30160014 ME30160015 ME30160016
- Product
- CAPNOSTREAM 20P (COV-INTL) N W/PRINTER ROHS, CS051COV
- Recalling firm
- Oridion Medical 1987 Ltd.
- Quantity
- 16
- Distribution
- The products were distributed US nationwide and Puerto Rico. The products were distributed to the following foreign countries: Argentina, Australia, Austria, Bahrain, Belgium, Canada, Columbia, Costa Rica, Croatia, Czech Republic, Denmark, Finland, France, Germany, Greece, Hungary, Ireland, Israel, Italy, Japan, Kazakhstan, Kuwait, Mexico, Netherlands, Norway, Oman, Pakistan, Panama, Peru, Philippines, Poland, Portugal, Qatar, Romania, Russia, Saudi Arabia, Serbia, Singapore, Slovakia, Slovenia, South Africa, Spain, Sweden, Switzerland, Thailand, Tunisia, Turkey, UAE, UK, and Vietnam.
- Recall date
- October 10, 2018
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)