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Heartstart defibrillation pads
Official notice
15 Dec 2022
Last checked
15 Dec 2022
An official Health Canada notice concerns Heartstart defibrillation pads. Some electrode pads used with the hs1/onsite/home AED have been observed to experience gel separation from the foam/tin backing when peeled from the yellow plastic liner. The gel may fold onto itself, resulting in reduced surface area of gel on the pad. A pad in this condition could cause the hs1/onsite/home AED to deliver less effective or ineffective therapy to the patient due to the reduced surface contact area with the skin. Recall start date: November 23, 2022 Published 2022-12-15.
What to do now
Contact the manufacturer if you require additional information.
Recall number
72333
Official notice
2022-12-15
The hazard
The hazard
Some electrode pads used with the hs1/onsite/home AED have been observed to experience gel separation from the foam/tin backing when peeled from the yellow plastic liner. The gel may fold onto itself, resulting in reduced surface area of gel on the pad. A pad in this condition could cause the hs1/onsite/home AED to deliver less effective or ineffective therapy to the patient due to the reduced surface contact area with the skin. Recall start date: November 23, 2022
How to check if you're affected
How to check if you're affected
Compare the product name and identifiers below with the item you own. Follow the official notice if they match.
Recall Numbers
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Affected products
Product 1
Risk / hazard
Where it was sold
Where it was sold
The source does not list specific retailers. See the official notice for where affected products were sold.
Location 1
Affected area 1
Company & contacts
Company & contacts
Brand: Philips, Heartstart Defibrillation Pads.
Source & status
Source & status
Source
Tier
Category
Classification
App estimate
Recall details
Recall details
Recall number
Classification
Source tier
Documents, notices & source
See the official notice and source documents for full details.
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