Health product recall

HEARTSTART DEFIBRILLATION PADS (2021-07-28)

Starting date:
July 28, 2021
Posting date:
August 10, 2021
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-76219

Last updated: 2021-08-10

Affected Products

HEARTSTART DEFIBRILLATION PADS

Reason

A problem has been identified in certain philips m5072a heartstart infant/child smart pads cartridges (lot y111220-01) which are used with the philips heartstart onsite and heartstart home automated external defibrillators (aeds). The problem is related to the graphic on the cover for the pads cartridge incorrectly showing application to an adult instead of a child.

Affected products

HEARTSTART DEFIBRILLATION PADS

Lot or serial number

Y111220-01

Model or catalog number

M5072A-ABA

Companies
Manufacturer
Philips Medical Systems
22100 Bothell Everett Highway
Bothell
98021
Washington
UNITED STATES