Maquet: Medical Device Recall in 2018 - (Recall #: Z-0490-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

Hemofiltration Standard Pack including BC 60 Plus-T 8036. Part Number: 701066990. Used in extracorporeal circulation during cardiopulmonary bypass procedures lasting 6 hours or less.

Product Classification:

Class II

Date Initiated: May 22, 2017

Date Posted: February 7, 2018

Recall Number: Z-0490-2018

Event ID: 78765

Reason for Recall:

55 kits were distributed after their expiration date of September 2015.

Status: Terminated

Product Quantity: 55 units

Code Information:

Lot/batch number: 3000001571 UDI code: 607567206489

Distribution Pattern:

Distributed to the states of NM, CA, and IL.

Voluntary or Mandated:

Voluntary: Firm initiated