Philips Medical Systems, Inc.: Medical Device Recall in 2015 - (Recall #: Z-1307-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

Lithium Polymer Fiber Optic Module Batteries used in the Intera MR System upgraded to CDAS, Part Number: 9065 and 9067. These rechargeable batteries are used to supply power to the following products: Wireless ECG Module used with the Precess MRI compatible Patient Monitoring System, Wireless SpO2 Module used with the Precess MRI Compatible Patient Monitoring System, Philips Basic Triggering Set, Philips Monitoring Sensor Set, Philips Battery Set

Product Classification:

Class II

Date Initiated: November 20, 2014

Date Posted: April 1, 2015

Recall Number: Z-1307-2015

Event ID: 69812

Reason for Recall:

VCG battery ignited in a VCG unit when recharging.

Status: Terminated

Product Quantity: 79

Code Information:

Batteries with date codes 2808 or earlier.

Distribution Pattern:

Distributed in the following states: AL, CA, FL, GA, IL, MA, MN, NC, ND, NE, NJ, NY, OH, OR, PA, TN, TX, UT, WA, WI; OUS: Australia, Austria, Belgium, China, Ecuador, Finland, France, Germany, Italy, Japan, Mexico, Netherlands, slovenia, South Africa, Sweden, Switzerland, United Kingdom

Voluntary or Mandated:

Voluntary: Firm initiated