HeartSine recalls specific defibrillator pads that may fail to analyze or deliver therapy due to depleted battery cells. Affected models include HeartSine Samaritan Public Access Defibrillators with certain serial numbers.
Single use battery and electrode cartridge may be rendered inoperable due to depleted battery cells which could prevent the defibrillator from analyzing patient condition or delivering therapy correctly.
HeartSine is recalling specific defibrillator pads that may not work properly because the battery cells are depleted. This could prevent the defibrillator from analyzing patient condition or delivering life-saving therapy correctly.
The single-use battery and electrode cartridges may become inoperable due to depleted battery cells. This could prevent the defibrillator from analyzing patient condition or delivering therapy correctly during a critical cardiac event.
Public access defibrillators used in emergencies, particularly those with the listed model numbers and serial numbers. Individuals with these specific pads are at risk if the defibrillator fails during a cardiac emergency.
Check if your HeartSine Samaritan Public Access Defibrillator has model numbers 350P/360P/450P/500P with the specific serial numbers listed in the recall notice. The pads are identified by the model and lot numbers provided in the recall record.
Identify your HeartSine Samaritan Public Access Defibrillator model (350P/360P/450P/500P) and check the serial numbers against the list provided in the recall notice.
If your pads match the recalled model and serial numbers, replace them with new, non-recalled pads to ensure proper defibrillator function.
The single-use battery and electrode cartridges may become inoperable due to depleted battery cells, which could prevent the defibrillator from analyzing patient condition or delivering therapy correctly.
Check if your HeartSine Samaritan Public Access Defibrillator model (350P/360P/450P/500P) has the specific serial numbers listed in the recall notice.
Replace the pads with new, non-recalled pads to ensure the defibrillator can function properly during an emergency.
We’ve drafted a message you can send HeartSine to request your refund or repair — edit it as you like.
Subject: Recall Z-2143-2023 — HeartSine HeartSine Hello, I own a HeartSine that is covered by recall Z-2143-2023 from HeartSine. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
