Maquet Cardiopulmonary Bypass Custom Tubing kit BEQ-TOP recall
Maquet Cardiopulmonary Bypass Custom Tubing kit BEQ-TOP 5909 14 Pack QPID, Part Number 701064992
Why was Maquet Cardiopulmonary Bypass Custom Tubing kit BEQ-TOP recalled?
There is a potential problem with the cuvette where failure of the cuvette would cause an error message on the monitor display of H/S DISCONNECT AT CUVETTE.
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?
Batch Number 3000018640, UDI Code 10607567205373; Batch Number 3000020516, UDI Code 10607567205373
- Product
- Maquet Cardiopulmonary Bypass Custom Tubing kit BEQ-TOP 5909 14 Pack QPID, Part Number 701064992
- Recalling firm
- Datascope Corporation
- Quantity
- 19 total kits
- Distribution
- The products were distributed to the following US states: AL, OR, and TX.
- Recall date
- June 13, 2018
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (device)