Draeger Medical, Inc.: Medical Device Recall in 2013 - (Recall #: Z-0939-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product Description:

Draeger Infinity Acute Care System (IACS) Monitoring Solution. Catalog Number MS20783 (Infinity MCable-Dual Hemo) Physiological patient monitoring system.

Product Classification:

Class II

Date Initiated: December 13, 2012

Date Posted: March 20, 2013

Recall Number: Z-0939-2013

Event ID: 64447

Reason for Recall:

The displayed value for the invasive blood pressure measurement of the IACS was different than the actual patient values. Liquid ingress in the cable connection may cause inaccurate measurements. This can happen if the Dual Hemo MCable is used in a non-vertical position, a vertical position but upside down, or laying it on the floor or on the patient bed.

Status: Terminated

Product Quantity: 260

Code Information:

Catalog Number MS20783 (Infinity MCable-Dual Hemo)

Distribution Pattern:

Distributed in the states of CA, IL, and MA.

Voluntary or Mandated:

Voluntary: Firm initiated