E SERIESRecalls & reported problems across all models
Zoll Medical Corporation · 160 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
E SERIES models — page 2
160 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- E SERIES 50000710010164013Automated external defibrillators (non-wearable)1 report
- E SERIES 50000730010064013Automated external defibrillators (non-wearable)1 report
- E SERIES 50001010010024013Automated external defibrillators (non-wearable)1 report
- E SERIES 50001010010164012Automated external defibrillators (non-wearable)1 report
- E SERIES 50001010020124013Automated external defibrillators (non-wearable)1 report
- E SERIES 50001010030124011Automated external defibrillators (non-wearable)1 report
- E SERIES 50001030010124013Automated external defibrillators (non-wearable)1 report
- E SERIES 50001310010164013Automated external defibrillators (non-wearable)1 report
- E SERIES 50001410030024013Automated external defibrillators (non-wearable)1 report
- E SERIES 50001310020164013Automated external defibrillators (non-wearable)1 report
- E SERIES 50001310020174013Automated external defibrillators (non-wearable)1 report
- E SERIES 50001330020124012Automated external defibrillators (non-wearable)1 report
- E SERIES 50001410020164013Automated external defibrillators (non-wearable)1 report
- E SERIES 50001710020064012Automated external defibrillators (non-wearable)1 report
- E SERIES 50001710020064013Automated external defibrillators (non-wearable)1 report
- E SERIES 50001710030124012Automated external defibrillators (non-wearable)1 report
- E SERIES 50001710030164013Automated external defibrillators (non-wearable)1 report
- E SERIES 50001810020164012Automated external defibrillators (non-wearable)1 report
- E SERIES 50001830030164013Automated external defibrillators (non-wearable)1 report
- E SERIES 50001730030124011Automated external defibrillators (non-wearable)1 report
- E SERIES 50001730030164013Automated external defibrillators (non-wearable)1 report
- E SERIES 50001740020124012Automated external defibrillators (non-wearable)1 report
- E SERIES 50001930030124013Automated external defibrillators (non-wearable)1 report
- E SERIES 50002730020124013Automated external defibrillators (non-wearable)1 report
- E SERIES 50002730030124013Automated external defibrillators (non-wearable)1 report
- E SERIES 50011310020064014Automated external defibrillators (non-wearable)1 report
- E SERIES 50011310020124014Automated external defibrillators (non-wearable)1 report
- E SERIES 50011330020164013Automated external defibrillators (non-wearable)1 report
- E SERIES 50011330030124013Automated external defibrillators (non-wearable)1 report
- E SERIES 50011340020124014Automated external defibrillators (non-wearable)1 report
- E SERIES 50011410020124012Automated external defibrillators (non-wearable)1 report
- E SERIES 50010730010124013Automated external defibrillators (non-wearable)1 report
- E SERIES 50011710020024013Automated external defibrillators (non-wearable)1 report
- E SERIES 50011710020064013Automated external defibrillators (non-wearable)1 report
- E SERIES 50011710030124011Automated external defibrillators (non-wearable)1 report
- E SERIES 50011720020024013Automated external defibrillators (non-wearable)1 report
- E SERIES 50011730020064013Automated external defibrillators (non-wearable)1 report
- E SERIES 50011810010124013Automated external defibrillators (non-wearable)1 report
- E SERIES 50011830020124012Automated external defibrillators (non-wearable)1 report
- E SERIES 50011830020174013Automated external defibrillators (non-wearable)1 report
- E SERIES 50011910020164013Automated external defibrillators (non-wearable)1 report
- E SERIES 50011930020164013Automated external defibrillators (non-wearable)1 report
- E SERIES 80000730010064013Automated external defibrillators (non-wearable)1 report
- E SERIES 80001310010124013Automated external defibrillators (non-wearable)1 report
- E SERIES 80001310010164013Automated external defibrillators (non-wearable)1 report
- E SERIES 80001310020164013Automated external defibrillators (non-wearable)1 report
- E SERIES 80001710010124012Automated external defibrillators (non-wearable)1 report
- E SERIES 80001710030124012Automated external defibrillators (non-wearable)1 report
- E SERIES 80001710030124013Automated external defibrillators (non-wearable)1 report
- E SERIES 80001730020124012Automated external defibrillators (non-wearable)1 report
- E SERIES 80001810020164013Automated external defibrillators (non-wearable)1 report
- E SERIES 80001930020124013Automated external defibrillators (non-wearable)1 report
- E SERIES 80011310020124014Automated external defibrillators (non-wearable)1 report
- E SERIES 80011730020124013Automated external defibrillators (non-wearable)1 report
- E SERIES 80011830020124014Automated external defibrillators (non-wearable)1 report
- E SERIES 80011930020124014Automated external defibrillators (non-wearable)1 report
- E SERIES 80011930020164013Automated external defibrillators (non-wearable)1 report
- E SERIES 80011930030124013Automated external defibrillators (non-wearable)1 report
- E SERIES 50011710010124013Automated external defibrillators (non-wearable)1 report
- E SERIES 50011810020064013Automated external defibrillators (non-wearable)1 report
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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