Heartstart Defibrillation Pads
Brand(s)
Summary
Contact the manufacturer if you require additional information.
Affected products
Affected products |
Lot or serial number |
Model or catalogue number |
---|---|---|
Heartstart Defibrillation Pads |
Not applicable |
M5071A |
Issue
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
Additional information
Details
Philips Medical Systems.
22100 Bothell Everett Highway, Bothell, Washington, United States, 98021