Datascope Corporation: Medical Device Recall in 2014 - (Recall #: Z-2568-2014)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

LINEAR 7.5 FR. 40cc IAB Catheter Maquet Getinge Group

Product Classification:

Class III

Date Initiated: August 11, 2014

Date Posted: September 10, 2014

Recall Number: Z-2568-2014

Event ID: 69072

Reason for Recall:

During label reconciliation a duplicate serial number label was detected to be printed for the LINEAR 7.5 FR 40 cc Intra-Aortic Balloon Catheter.

Status: Terminated

Product Quantity: one unit

Code Information:

Part Number - 0684-00-0480-01U

Distribution Pattern:

US Distribution to TX.

Voluntary or Mandated:

Voluntary: Firm initiated