Maquet Cardiopulmonary Bypass Custom Tubing kit BO-TOP recall
Maquet Cardiopulmonary Bypass Custom Tubing kit BO-TOP 38600 ADULT CPB, Part Number 701056035R01 Product Usage: The Maquet Cardiopulmonary Bypass…
Why was Maquet Cardiopulmonary Bypass Custom Tubing kit BO-TOP recalled?
There is a potential for the over-pressure safety (OPS) valve in the tubing kits to not allow flow through.
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?
UDI 0607567210004
- Product
- Maquet Cardiopulmonary Bypass Custom Tubing kit BO-TOP 38600 ADULT CPB, Part Number 701056035R01 Product Usage: The Maquet Cardiopulmonary Bypass…
- Recalling firm
- Datascope Corporation
- Quantity
- 8
- Distribution
- The products were distributed to the following US states: IA and FL.
- Recall date
- June 20, 2018
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)