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.
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.
The sets have connectors assembled in reverse order, causing blue (venous) to connect with red (arterial) lines. This incorrect setup prevents the device from being primed properly before use, which could lead to improper function during medical procedures.
Healthcare professionals using the specific Maquet Cardiopulmonary Set Advanced 7.0 model BEQ-HLS-7050 are most at risk if they attempt to use the set without proper priming.
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.
Verify the model number BEQ-HLS-7050 and part number 701052794 on the set.
The sets were assembled with reversed connectors, which prevents proper priming before use and may cause the device to not function correctly.
The recall record does not specify a remedy, so no action is required beyond checking if your set matches the model and part numbers.
Look for model number BEQ-HLS-7050 and part number 701052794. Affected units also have lot number 70131093 and unique device identifier 04037691741543.
We’ve drafted a message you can send Maquet to request your refund or repair — edit it as you like.
Subject: Recall Z-2149-2019 — Maquet Maquet Hello, I own a Maquet that is covered by recall Z-2149-2019 from Maquet. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.
