Maquet Cardiovascular, LLC: Medical Device Recall in 2023 - (Recall #: Z-0589-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

Acrobat-i Vacuum Positioner System, Model Number XP-5000Z

Product Classification:

Class II

Date Initiated: October 31, 2023

Date Posted: December 27, 2023

Recall Number: Z-0589-2024

Event ID: 93477

Reason for Recall:

The Positioner Arm may not tighten or lock during normal use.

Status: Ongoing

Product Quantity: 6472 units

Code Information:

UDI-DI: 00607567500006; Lot Numbers: 3000195267, 3000195268, 3000195273, 3000195663, 3000199248, 3000199725, 3000204637, 3000207240, 3000211594, 3000212053, 3000213219, 3000214053, 3000214054, 3000214255, 3000221064, 3000214052, 3000225770, 3000226531, 3000225866, 3000225769, 3000231209, 3000231210

Distribution Pattern:

US Nationwide. Global Distribution.

Voluntary or Mandated:

Voluntary: Firm initiated