Philips is notifying customers of a potential issue with the Adult SMART Pads Cartridge (M5071A) and the Infant/Child SMART Pads Cartridge (M5072A) for use specifically with the HeartStart HS1 AEDs.
Philips has identified that for affected pads, some gel may fold onto itself, resulting in reduced surface area of gel on the pad, or it may separate almost completely leaving only a small amount of gel on the pad to make contact with a patient’s skin.
If this occurs, the HS1 AED could deliver less effective or ineffective therapy. As affected pads are stored in sealed cartridges, this issue will not be visible until the cartridge is opened for use. Users should continue to use the HS1 AED and pads as-is and follow the device’s voice prompts during use. The AED will audibly guide users through each step of the procedure. It is recommended that customers and users keep their HS1 AED in service according to the Instructions for Use/Owner’s Manual.
Philips is actively working on design changes to eliminate this issue in the Adult SMART Pads Cartridge and the Infant/Child SMART Pads Cartridge, and projects new pad availability later in 2022. Affected customers will be notified when the new design pad is available. This issue only relates to HeartStart HS1 AEDs and does not involve HeartStart FRx.
Key Points
During use, ensure the majority of the pad surface is covered with gel and apply the pads to the patient. If you notice the gel beginning to separate from the foam backing as you peel, try to prevent the gel from folding onto itself if possible. Do not hesitate to apply the pads to the patient unless the gel has almost completely separated from the backing. In case of trouble, install spare pads if available and continue the rescue. No matter the state of the pads, follow the voice prompts because the AED will walk you through the necessary actions.
It is not possible to know if your pads are affected by the problem prior to use because the pads are protected by a foil seal. The foil seal on the pads cartridge should be opened only for patient use in an emergency because the pads will quickly dry out if the foil seal is broken.
Once you receive the updated Adult SMART pads cartridge, replace the current pads cartridge in your AED with the new one. The current pads cartridge LOT # starts with a Y. Where to find the LOT #:
After the updated pads have been installed in the AED, please discard all pads cartridges in your possession with a LOT number beginning with “Y”.
Philips recommends that you store a spare pads cartridge with your HS1 AED. If you need to change your pads in an emergency, there is a short video showing how to replace the pads cartridge at:
www.philips.com/replace-aed-pads
Please pass the notice to all those who need to be aware within your organization or to any organization where HS1 AED devices or pads cartridges have been transferred, (if appropriate.)
Keep a copy of your letter with the Instructions for Use/Owner’s Manual of your HS1 AED.
Philips is issuing a Field Safety Notice regarding the Adult SMART Pads Cartridge [REF: M5071A] and the Infant/Child SMART Pads Cartridge [REF: M5072A] for use with the HeartStart HS1, Automated External Defibrillator (AED) devices. The HeartStart HS1 AEDs are intended for use in public places or the home.
HS1 AED pads (PN: M5071A, M5072A) 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, or it may separate almost completely leaving only a small amount of gel on the pad. Any pad currently installed in or stored with an HS1 AED could experience this problem, and it is not possible to know prior to patient use if your pad is affected because the pads are protected by a foil seal. At the time of the issuance of the February 2022 notification, Philips has received 100 reports about this issue since 2010 out of approximately 5 million shipments of M5071A and M5072A pads. (Most of these reports, approximately 80, were received in 2021.)
No. Users should continue to use the HS1 AED and pads as-is, and follow the device’s voice prompts during use, because the AED will audibly guide users through each step of the procedure. It is recommended that customers and users keep their HS1 AED in service according to the Instructions for Use/Owner’s Manual and the Letter/Field Safety Notice.
In the event of significant loss of gel, there is a possibility that the pad may not adhere correctly, or not make effective contact with a patient’s skin. Should this occur, there is a possibility of insufficient therapy delivery, or of patient skin burns. There is also the potential for delayed therapy, if the appearance of the peeled pad leads a user to not use affected pads and/or spend time searching for spare pads.
Users should continue to use the HS1 AED and pads as-is, and follow the device’s voice prompts during use, because the AED will audibly guide users through each step of the procedure. It is recommended that customers and users keep their HS1 AED in service according to the Instructions for Use/Owner’s Manual and the Field Safety Notice.
Any HS1 AED pad (PN:M5071A, M5072A) currently installed in or stored with an HS1 AED could experience this issue. It is not possible to know prior to patient use if a pad is affected because the pads are protected by a foil seal.
At the time of the February 2022 issuance of this notification, Philips has received approximately 100 reports about this issue out of approximately 5 million shipments of M5071A and M5072A pads since 2010. (Most of these reports, approximately 80, were received in 2021.)
IMPORTANT NOTE: The issue described in the Field Service Notice does not affect the FRx device and pads.
Users should continue to use the HS1 AED and pads as-is, and follow the device’s voice prompts during use, because the AED will audibly guide users through each step of the procedure. It is recommended that customers and users keep their HS1 AED in service according to the Instructions for Use/Owner’s Manual and the Field Safety Notice.
A discolored, melted appearance does not have any impact on the delivery of therapy; however, there may be a delay of therapy if the user hesitates to apply the pad due to its' appearance.
Do not hesitate to apply discolored, melted pads to the patient unless the gel has almost completely separated from the backing. No matter the state of the pads, the HS1 AED will audibly prompt the user through each step of the procedure.
As described in the Instructions For Use (IFU), it is recommended that you store a spare pads cartridge with your HS1 AED. A short video showing how to replace the pads cartridge can be found at: www.philips.com/replace-aed-pads-video
Locate the latch at the top edge of the AED and slide it to the side. The SMART pads cartridge will be released. Lift out the used SMART pads cartridge. Insert the bottom end of the new SMART Pads cartridge into the recess, then press in the cartridge until the latch clicks into place. You can view a short video showing how to replace the pads cartridge at the following web address. www.philips.com/replace-aed-pads-video
Philips is working on changes intended to eliminate the issue in the M5071A and M5072A pads, including updates to production processes and changes to the pad composition.
Philips is working on changes intended to eliminate the issue in M5071A and M5072A pads. Philips expects to release updated pads later in 2022.
No, this issue only affects Adult SMART Pads Cartridge [REF: M5071A] and the Infant/Child SMART Pads Cartridge [REF: M5072A] for use with the HeartStart HS1 Automated External Defibrillator (AED) devices.
The issue described in the Field Service Notice does not affect the Philips FRx device and pads. Philips continues to fulfill orders for the FRx AED and accessories including SMART Pads II.
The relevant regulatory authorities were notified of this issue in February 2022.
Customers may contact their local Philips Representative as shown in the Field Service Notice.
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