FDAClass IIJune 5, 2019

Maquet Getinge-BEQ-T 5211 LARGE ECC SET recall: Sterility Concern

Maquet Getinge-BEQ-T 5211 LARGE ECC SET Material:701064560

Why was Maquet Getinge-BEQ-T 5211 LARGE ECC SET 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: Batch 3000041128 3000045731 3000050577 3000052947 3000054617 3000054955 3000057631 3000071818

Product
Maquet Getinge-BEQ-T 5211 LARGE ECC SET Material:701064560
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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