FDAClass IIJune 5, 2019

Maquet Getinge-BEQ-TOP 24105 ECC PACK recall: Sterility Concern

Maquet Getinge-BEQ-TOP 24105 ECC PACK Material:701064757

Why was Maquet Getinge-BEQ-TOP 24105 ECC PACK 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: 3000051271 3000057632 3000062460 3000066202 3000069076 3000073425 3000076761 3000080703

Product
Maquet Getinge-BEQ-TOP 24105 ECC PACK Material:701064757
Recalling firm
Maquet Cardiovascular, LLC
Quantity
N/A
Distribution
Nationwide
Recall date
June 5, 2019
Classification
Class II
Status
Terminated
Agency
FDA (device)
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