FDA Recall Terminated

GE Healthcare, ApexPro Telemetry System The ApexPro Telemetry System is intended for use under the direct supervision of a licensed healthcare practitioner. The system is designed to acquire and monitor physiological data for ambulating patients within a defined coverage area. The system processes this physiological data to detect various ECG arrhythmia events and select physiological parameter limit violations. The ApexPro Telemetry System is intended to be installed in the hospital or clinical environment in order to provide clinicians with patient physiological data, while allowing for patient mobility. These systems are typically deployed in sub acute care areas in hospitals or clinical sites where patient mobility can enhance the effectiveness of the medical procedures administered. The physiological parameters monitored include ECG, noninvasive blood pressure, non-invasive temperature and SpO2. The ApexPro Telemetry System is intended to provide ECG data via Ethernet to the computer platform for processing. The ApexPro Telemetry System is also intended to provide physiologic data over the Unity Network to clinical information systems for display.

Recall: Z-1522-2011 · Initiated January 28, 2011

Recall

Recall Number
Z-1522-2011
Event Number
56660
Firm
GE Healthcare, LLC
FEI Number
2126677
Product Code
MHX
Status
Terminated
Root Cause
Software design
Initiated
January 28, 2011
Posted
March 3, 2011
Terminated
May 29, 2012
Address
3000 N Grandview Blvd, Waukesha, WI, 53188-1615

Description

GE Healthcare, ApexPro Telemetry System The ApexPro Telemetry System is intended for use under the direct supervision of a licensed healthcare practitioner. The system is designed to acquire and monitor physiological data for ambulating patients within a defined coverage area. The system processes this physiological data to detect various ECG arrhythmia events and select physiological parameter limit violations. The ApexPro Telemetry System is intended to be installed in the hospital or clinical environment in order to provide clinicians with patient physiological data, while allowing for patient mobility. These systems are typically deployed in sub acute care areas in hospitals or clinical sites where patient mobility can enhance the effectiveness of the medical procedures administered. The physiological parameters monitored include ECG, noninvasive blood pressure, non-invasive temperature and SpO2. The ApexPro Telemetry System is intended to provide ECG data via Ethernet to the computer platform for processing. The ApexPro Telemetry System is also intended to provide physiologic data over the Unity Network to clinical information systems for display.

Reason

GE Healthcare has become aware of a potential for loss of patient monitoring when ApexPro Telemetry System is used in conjunction with a mirrored view CARESCAPE CIC Pro in combination monitoring mode (combo mode). The safety issue includes the potential for a delay in annunciation of audible alarms when used in combo mode, and may result in the delay of treatment of a cardiac event.

Action

GE sent an "Urgent Medical Device Correction" letter dated December 29, 2010. The letter was addressed to Healthcare Administrator / Risk Manger, Chief of Nursing and Director of Biomedical Engineering. The letter described the Safety Issue, Affected Product Details, Product Correction, Safety Instruction and Contact Information. Customers were instructed to contact Technical Support or their local Service Representative with any questions regarding this medical device. For any questions regarding this recall call 262-573-4122.

Distribution

Worldwide Distribution - USA including AL, AK, AZ, AR, CA, CO, CT, DC, FL, GA, HI, ID, IL, IN, IA, KS, KY, LA, ME, MD, MA, MI, MN, MS, MO,MT,NE, NJ, NM, NY, NC, OH, OK, OR, PA, PR, SC, TN, TX, UT, VT, VA, WA, WV, WI, WY. and the UNITED KINGDOM, THAILAND, SWITZERLAND, SWEDEN, SPAIN, SOUTH KOREA, RUSSIA, NORWAY, NEW ZEALAND, NETHERLANDS, MALAYSIA, JAPAN, ITALY, ISRAEL, IRELAND, GERMANY, FRANCE, FINLAND, DENMARK, CUBA, CHINA, CANADA, AUSTRIA, AUSTRALIA, POLAND.

Quantity

2346