QUADROX-iR, used during cardiopulmonary bypass Model Item No. Description BEQ-HMO 51100-USA 701067936 Small Adult with filter, with BIOLINE coating BEQ-HMO 71100-USA 701067880 Adult with filter, with BIOLINE Coating HMO 50100-USA 701067934 Small Adult without filter, with SOFTLINE Coating HMO 51100-USA 701067938 Small Adult with filter, with SOFTLINE Coating HMO 70100-USA 701067874 Adult without filter, with SOFTLINE Coating HMO 71100-USA 701067886 Adult with filter, with SOFTLINE Coating
FDA Recall Z-1662-2023 · Posted 2023-05-30
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Recalling FirmMaquet Medical Systems USA
Recall StatusOpen, Classified
Product CodeDTZ
Date Initiated2023-05-18
Product Quantity0 (US)
Reason for Recall
Product packaging may exhibit small pinholes which may not be visible to the unaided eye, compromising the sterile barrier of the packaging. Exposure to non-sterile device may result in inflammation, infection, sepsis, and ischemia.
Firm Action
On May 18, 2023, the firm notified customers of the recall via an Urgent Medical Device Removal letter.
Actions to be taken by the customer:
If an affected device is already in use, please use according to normal practices.
Monitor the patient for signs and symptoms of inflammation, infection, sepsis, and ischemia. If detected, treat according to clinical protocols.
Please remove any affected product in inventory from areas of use. Unopened and unexpired affected product is eligible for credit upon return.
Product Return: Please contact Getinge Customer Service at 1-888-943-8872 option 2 between the hours of 6:00 AM and 5:00 PM Pacific Standard Time to request a return authorization (RMA) and shipping instructions to return any affected product.
Distributors who have shipped affected products to customers should forward the notification to customers' attention for appropriate action.
Maquet Cardiopulmonary GmbH is working with all possible urgency on the redesign and revalidation of a packaging solution, which is anticipated to be available by Q4 2023.
Root Cause
Under Investigation by firm
Distribution Pattern
Nationwide domestic distribution
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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