Capnostream20 recall
Capnostream20 (US) N REFURBISHED, Part Number CS78651
Why was Capnostream20 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?
B200001005 B200001300 B200001477 B200001546 B200001548 B200001557 B200001560 B200001582 B200001583 B200001591 B200001598 B200001601 B200001603 B200001606 B200001631 B200001641 B200001817 B200001884 B200001920 B200001938 B200001977 B200001986 B200002051 B200002060 B200002070 B200002078 B200002134 B200002148 B200002163 B200001387 B200001569 B200001673 B200001679 B200001844 B200002025 B200002031 B200002145 B200001827 B200001137 B200001160 B200001310 B200001660 B200001872 B200002187 B400002132 B200001671
- Product
- Capnostream20 (US) N REFURBISHED, Part Number CS78651
- Recalling firm
- Oridion Medical 1987 Ltd.
- Quantity
- 46
- 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)