Maquet Cardiovascular Us Sales, Llc: Medical Device Recall in 2016 - (Recall #: Z-1373-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

Rotaflow Centrifugal Pump Custom tubing packs for the oxygenator

Product Classification:

Class II

Date Initiated: February 23, 2016

Date Posted: April 20, 2016

Recall Number: Z-1373-2016

Event ID: 73390

Reason for Recall:

Maquet Cardiopulmonary (MCP) is conducting a voluntary recall based on the potential risk of exposure to endotoxin for various products.

Status: Terminated

Product Quantity: 72,000 units in total

Code Information:

BEQ-RF32, BEQ-RF-32-USA, BO-RF-32, BO-RF-32 USA, RF-32, RF-32 USA, RF-32u.

Distribution Pattern:

US Nationwide Distribution.

Voluntary or Mandated:

Voluntary: Firm initiated