Reported Jul 10, 2019 · Ongoing
ZOLL AED PRO Automated External Defibrillator Product Usage: The AED PRO unit is intended to defibrillate victims of…
ZOLL Medical Corporation
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: ZOLL Medical Corporation · 269 & 271 Mill Road · Chelmsford, MA · 01824
Is this the product you have?
- ZOLL AED PRO Automated
- External Defibrillator Product UsageThe AED PRO unit is intended to defibrillate victims of ventricular fibrillation or pulseless ventricular tachycardia, for ECG monitoring, and for CPR monitoring of patients. The CPR monitoring function provides a metronome designed to encourage rescuers to perform chest compressions at the AHA/ERC recommended rate of 100 compressions per minute. Voice and visual prompts encourage a compression depth of at least 2 inches (5 cm) for adult patients. The AED PRO system is indicated for use on victims of cardiac arrest with apparent
- lack of circulation as indicated byUnconsciousness Absence of breathing, and Absence of pulse and other signs of circulation. The device is also indicated for use when ECG monitoring is indicated to evaluate the patient s heart rate or ECG morphology. The AED PRO system is indicated for adult and pediatric patients
- Lot codes and dates
- Part Numbers
9001020049999101090010400499991010700104004999910109001020249999101090010600499991010
- GTIN
0084794601612800847946016142008479460151380084794601613500847946016166
- Serial Numbers
1,969 of 1,969 codes
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
- Part Numbers
- Amount recalled
- 1,969
Where it was sold
- Nationwide
Why it was recalled
There is a potential for the device to fail to deliver energy to the patient.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
Free recall alerts
Get alerted about new ZOLL Medical Corporation recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.