Maquet Getinge-BO-T 2303 Small Adult Cardiac Surgery recall: Sterility Concern
Maquet Getinge-BO-T 2303 Small Adult Cardiac Surgery Material:709000004
Why was Maquet Getinge-BO-T 2303 Small Adult Cardiac Surgery recalled?
Custom Tubing Sets for Extracorporeal Circulation (ECC)-During sterilization, the closed stopcock/non-vented cap configuration may prevent the flow of humidity/ethylene oxide gas into the fluid-path between the closed port and the non-vented cap therefore the Sterility Assurance Level (SAL) of the stopcock ports cannot be assured
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 Numbers: 3000045083 3000046399
- Product
- Maquet Getinge-BO-T 2303 Small Adult Cardiac Surgery Material:709000004
- Recalling firm
- Maquet Cardiovascular, LLC
- Quantity
- N/A
- Distribution
- Nationwide
- Recall date
- June 5, 2019
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)