ZOLL Medical Corporation recalls AED PRO devices that may fail to deliver energy to patients during cardiac arrest. Affected units have specific serial numbers and part numbers listed. Users should stop using and contact ZOLL for replacement.
There is a potential for the device to fail to deliver energy to the patient.
ZOLL is recalling its AED PRO Automated External Defibrillator units that may fail to deliver energy to patients during cardiac arrest. This could be dangerous if the device doesn't work when needed. Affected units have specific serial numbers and part numbers listed in the recall.
The device may fail to deliver the necessary electrical energy to the patient during a cardiac arrest event. This could prevent the device from effectively treating a life-threatening condition, potentially leading to death or serious injury if the patient's heart stops.
People who own or use the ZOLL AED PRO devices with the listed serial numbers or part numbers are affected. Emergency responders and first aid providers are at the highest risk.
Check your ZOLL AED PRO device for the listed serial numbers (e.g., AA17C041915) or part numbers (e.g., 90010200499991010) to see if it's affected. The recall includes specific serial numbers and part numbers provided in the notice.
Immediately stop using the affected ZOLL AED PRO device if you own or use it. The device may fail to deliver energy during cardiac arrest.
Reach out to ZOLL Medical Corporation for instructions on how to get a replacement or repair.
The ZOLL AED PRO is an Automated External Defibrillator designed to treat cardiac arrest by delivering electrical energy to the heart.
Check your device's serial number against the list of affected serial numbers (e.g., AA17C041915) or part numbers (e.g., 90010200499991010) provided in the recall notice.
Yes, the device may fail to deliver energy during cardiac arrest, which could lead to death or serious injury if the patient's heart stops.
We’ve drafted a message you can send ZOLL to request your refund or repair — edit it as you like.
Subject: Recall Z-1931-2019 — ZOLL ZOLL Hello, I own a ZOLL that is covered by recall Z-1931-2019 from ZOLL. 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.
