X SERIESRecalls & reported problems across all models
Zoll Medical Corporation · 163 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
X SERIES models — page 2
163 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- X SERIES 600-2241511-01Automated external defibrillators (non-wearable)3 reports
- X SERIES 600-2231011-01COMPUTER, BLOOD-PRESSURE3 reports
- X SERIES 610-0220510-01Automated external defibrillators (non-wearable)3 reports
- X SERIES 620-0210001-01Automated external defibrillators (non-wearable)3 reports
- X SERIES 620-0220001-01Automated external defibrillators (non-wearable)3 reports
- X SERIES 620-0220010-01Automated external defibrillators (non-wearable)3 reports
- X SERIES 620-2120011-01Automated external defibrillators (non-wearable)3 reports
- X SERIES 620-2231001-01Automated external defibrillators (non-wearable)3 reports
- X SERIES 620-2241511-01Automated external defibrillators (non-wearable)3 reports
- X SERIES 610-2231510-01Automated external defibrillators (non-wearable)2 reports
- X SERIES 610-2230011-01Automated external defibrillators (non-wearable)2 reports
- X SERIES 600-0221511-01Automated external defibrillators (non-wearable)2 reports
- X SERIES 600-2221410-01Automated external defibrillators (non-wearable)2 reports
- X SERIES 620-0241511-01Automated external defibrillators (non-wearable)2 reports
- X SERIES 620-2121011-01Automated external defibrillators (non-wearable)2 reports
- X SERIES 620-2221001-01Automated external defibrillators (non-wearable)2 reports
- X SERIES 620-2230011-01Automated external defibrillators (non-wearable)2 reports
- X SERIES 620-2271011-01Automated external defibrillators (non-wearable)2 reports
- X SERIES 620-2261411-01Automated external defibrillators (non-wearable)2 reports
- X SERIES 630-2271111-01Automated External Defibrillators (Non-Wearable)2 reports
- X SERIES 620-2441511-01-66Automated external defibrillators (non-wearable)1 death2 reports
- X SERIES 610-0210511-01Automated external defibrillators (non-wearable)2 reports
- X SERIES 610-2251511-01Automated external defibrillators (non-wearable)2 reports
- X SERIES 610-2261511-01Automated external defibrillators (non-wearable)2 reports
- X SERIES 610-2120011-01Automated external defibrillators (non-wearable)1 report
- X SERIES 610-2121010-01Automated external defibrillators (non-wearable)1 report
- X SERIES 610-2211011-01Automated external defibrillators (non-wearable)1 report
- X SERIES 610-2220010-01Automated external defibrillators (non-wearable)1 report
- X SERIES 610-2220011-01Automated external defibrillators (non-wearable)1 report
- X SERIES 600-2241511-01-66Automated external defibrillators (non-wearable)1 report
- X SERIES 600-1221511-01Automated external defibrillators (non-wearable)1 report
- X SERIES 600-2220010-01Automated external defibrillators (non-wearable)1 report
- X SERIES 600-2221010-01Automated external defibrillators (non-wearable)1 report
- X SERIES 600-2231411-01Automated external defibrillators (non-wearable)1 report
- X SERIES 600-2231511-01Automated external defibrillators (non-wearable)1 report
- X SERIES 610-0120011-01Automated external defibrillators (non-wearable)1 report
- X SERIES 610-0121511-01Automated external defibrillators (non-wearable)1 report
- X SERIES 610-0120001-01Automated external defibrillators (non-wearable)1 report
- X SERIES 610-0221511-01-66Automated external defibrillators (non-wearable)1 report
- X SERIES 610-2211511-01-66Automated external defibrillators (non-wearable)1 report
- X SERIES 620-0221411-01Automated external defibrillators (non-wearable)1 report
- X SERIES 620-0230011-01Automated external defibrillators (non-wearable)1 report
- X SERIES 620-0231011-01Automated external defibrillators (non-wearable)1 report
- X SERIES 620-2220011-01Automated external defibrillators (non-wearable)1 report
- X SERIES 620-2230411-01Automated external defibrillators (non-wearable)1 report
- X SERIES 620-2231010-01Automated external defibrillators (non-wearable)1 report
- X SERIES 620-2131011-01-66Automated external defibrillators (non-wearable)1 report
- X SERIES 620-0221301-01Automated external defibrillators (non-wearable)1 report
- X SERIES 620-2221311-01Automated external defibrillators (non-wearable)1 report
- X SERIES 620-2221411-01-66Automated external defibrillators (non-wearable)1 report
- X SERIES 620-2221011-01-68Automated external defibrillators (non-wearable)1 report
- X SERIES 620-0220311-01Automated external defibrillators (non-wearable)1 report
- X SERIES 630-2221211-01Automated External Defibrillators (Non-Wearable)1 report
- X SERIES 631-2271211-01Automated External Defibrillators (Non-Wearable)1 report
- X SERIES 630-2131111-01Automated External Defibrillators (Non-Wearable)1 report
- X SERIES 630-2230111-01Automated External Defibrillators (Non-Wearable)1 report
- X SERIES 630-2441211-01Automated External Defibrillators (Non-Wearable)1 report
- X SERIES 630-2221111-01-68Automated external defibrillators (non-wearable)1 report
- X SERIES 620-0221511-01-68Automated external defibrillators (non-wearable)1 report
- X SERIES 631-2221111-01Automated External Defibrillators (Non-Wearable)1 report
- X SERIES 610-0220001-01Automated external defibrillators (non-wearable)1 report
- X SERIES 610-0210001-01Automated external defibrillators (non-wearable)1 report
- X SERIES 610-2441511-36Automated 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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