Brand

Philips Medical Systems North America Inc. Recalls

3 recalls on record. Search official CPSC, FDA, and USDA datasets for every recall issued for Philips Medical Systems North America Inc..

3Total Recalls
0Critical
1,824Units Affected
Feb 28, 2014Most Recent
All Recalls

Every Philips Medical Systems North America Inc. Recall

Sorted by most recent. Click any recall for full details.

3 recalls
High RiskFDA
Philips Medical Systems North America Inc.
Philips Model EPIQ 7 Ultrasound System. Intended for diagnostic ultrasound imaging and fluid flow analysis. Catalogue numbers 795200 ...
Cardiac Devices·1,267 affected·Feb 28, 2014
High RiskFDA
Philips Medical Systems North America Inc.
Philips HeartStart FR3 Automated External Defibrillator (AED), models 861388 and 861389. The HeartStart FR3 is a battery powered autom...
Cardiac Devices·251 affected·Feb 6, 2014
High RiskFDA
Philips Medical Systems North America Inc.
EPIQ 7 Ultrasound System, Model 795200, 795201, 795202. Intended for diagnostic ultrasound imaging and fluid flow analysis.
Diagnostic Devices·306 affected·Oct 17, 2013