FDAClass IIJune 5, 2019

Maquet Getinge-BEQ-TOP 24500 ADULT ECC Material recall: Sterility Concern

Maquet Getinge-BEQ-TOP 24500 ADULT ECC Material: 701050253

Why was Maquet Getinge-BEQ-TOP 24500 ADULT ECC Material 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: 3000041126 3000053053 3000054958 3000055326 3000064943 3000066814 3000071782

Product
Maquet Getinge-BEQ-TOP 24500 ADULT ECC Material: 701050253
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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