Maquet Cardiovascular Us Sales, Llc Maquet Cardiopulmonary (MCP)/Getinge HLS Set Advanced 7.0. Model Number BEQ-HLS-7050 USA, Part Number 701052794 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Maquet Cardiopulmonary (MCP)/Getinge HLS Set Advanced 7.0. Model Number BEQ-HLS-7050 USA, Part Number 701052794
Brand
Maquet Cardiovascular Us Sales, Llc
Lot Codes / Batch Numbers
Lot 70131093, UDI 04037691741543
Products Sold
Lot 70131093; UDI 04037691741543
Maquet Cardiovascular Us Sales, Llc is recalling Maquet Cardiopulmonary (MCP)/Getinge HLS Set Advanced 7.0. Model Number BEQ-HLS-7050 USA, Part Numbe due to 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 . Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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.
Recommended Action
Per FDA guidance
Urgent Medical Device Recall - Removal notification letters dated 7/11/19 were sent to customers.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
AR, CA, FL, GA, IL, IN, IA, KY, NE, NV, NM, NY, NC, OH, OR, TN, WI
Page updated: Jan 10, 2026