HeartStart FR3. Defibrillator (2018-10-02)
- Starting date:
- October 2, 2018
- Posting date:
- November 2, 2018
- Type of communication:
- Medical Device Recall
- Subcategory:
- Medical Device
- Hazard classification:
- Type II
- Source of recall:
- Health Canada
- Issue:
- Medical Devices
- Audience:
- General Public, Healthcare Professionals, Hospitals
- Identification number:
- RA-68188
Affected products
HeartStart FR3. Defibrillator
Reason
The recalled AEDs may not meet their IPx5 water ingress performance specification.
Affected products
HeartStart FR3. Defibrillator
Lot or serial number
begin with C16J, C16K, C17A & C17B
Model or catalog number
861388
Companies
- Manufacturer
-
Philips Medical Systems
22100 Bothell Everett Highway
Bothell
98021
UNITED STATES