Overview of recall records associated with Philips Electronics North America Corp., including dates, categories and classifications where available.
Classification mix: Class II: 3.
Automated external defibrillators may not fully meet IPx5 water ingress specification. The device may fail to function should water intrusion occur.
An issue with one of the electric components (a resistor) could result in the device not delivering a shock when needed.
An issue with one of the electric components (a resistor) could result in the device not delivering a shock when needed.
This page summarizes recall records in which the official source identifies Philips Electronics North America Corp. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.
