Lower riskMedical device recall · FDA · Published July 11, 2019
Maquet Cardiopulmonary Set 7.0: Incorrect Assembly Risk
Maquet recalls specific cardiopulmonary sets due to reversed connectors causing improper priming and potential device malfunction. Affected units have model BEQ-HLS-7050 and part number 701052794.
The sets are configured with quick connectors that have been assembled in reverse on the arterial and venous lines, resulting in blue (venous) to red (arterial) and red (arterial) to blue (venous) connections. Due to this incorrect assembly, the sets cannot be primed from the reservoir prior to use, and the device may not function as intended.
Take action
Contact the company
📍Recalling firmMaquet Cardiovascular Us Sales, Llc45 Barbour Pond Dr · Wayne, NJ 07470-2094
✎ GovInfoNow plain-language explainer
Maquet is recalling certain cardiopulmonary sets because they were assembled with reversed connectors. This means the sets can't be properly primed before use, which might cause the device to not work correctly during medical procedures. Read more at govinfonow.com/recall/67437-maquet-cardiopulmonary-set-7-0-incorrect-assembly-risk.
“Maquet Cardiopulmonary Set 7.0: Incorrect Assembly Risk.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/67437-maquet-cardiopulmonary-set-7-0-incorrect-assembly-risk. Based on FDA recall #Z-2149-2019 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2149-2019%22&limit=1).
The FDA announced on July 11, 2019, that Maquet Cardiovascular Us Sales, Llc is recalling the Maquet Cardiopulmonary (MCP)/Getinge HLS Set Advanced 7.0 due to incorrect assembly of quick connectors. This defect prevents the sets from being primed and may cause the device to malfunction.
How to tell if you have it
Brand: Maquet
Product: Maquet Cardiopulmonary (MCP)/Getinge HLS Set Advanced 7.0
Model Number: BEQ-HLS-7050 USA
Part Number: 701052794
Lot Code: 70131093
UDI: 04037691741543
The hazard
The sets feature quick connectors assembled in reverse on the arterial and venous lines, resulting in blue to red and red to blue connections. Due to this incorrect assembly, the sets cannot be primed from the reservoir prior to use, and the device may not function as intended.
Context
GovInfoNow's records show Maquet Cardiovascular Us Sales, Llc has had 14 other recalls since October 25, 2018. Other recent recalls of similar products include Maquet HLS Set Advanced 5.0 Recall (November 20, 2020), Maquet BMU 40 Blood Monitor Recall (September 30, 2020), and Maquet Yuno Mobile Operating Table Recall (September 24, 2020). Other recent recalls of similar products include Medline Medical Procedure Kits Recall (May 4, 2026) and Medline Medical Procedure Kits: Catheter Issues May Cause Premature Detachment (May 4, 2026).
How to tell if you have this one
Check for model number BEQ-HLS-7050 and part number 701052794 on the set. The affected units also have lot number 70131093 and unique device identifier 04037691741543.
Brand
Maquet
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Product Details
Verify the model number BEQ-HLS-7050 and part number 701052794 on the set.
Where it went and when
Where it was distributed
Distributed in 17 states.
Listed by the agency
Not listed
FDA distribution: “The products were distributed to the following US states: AR, CA, FL, GA, IA, IL, IN, KY, NC, NE, NM, NV, NY, OH, OR, TN, and WI.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Arkansas, California, Florida, Georgia, Illinois, Indiana, Iowa, Kentucky, Nebraska, Nevada, New Mexico, New York, North Carolina, Ohio, Oregon, Tennessee, Wisconsin.
Recall timeline
FDA terminated this recall 17 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-2149-2019 (July 11, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2149-2019 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.