Defibtech recalls
Defibtech has 14 recalls on record with the FDA and USDA, the earliest in 2020 and the latest reported on 7 May 2025. 11 are still ongoing.
Total recalls14since 2020
Last 12 months0reported
Class I17% of total
Ongoing11latest 7 May 2025
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 1 7%Class II 13 93%Class III 0 0%
Why defibtech is recalled
Product types
By year
Ongoing defibtech recalls
11 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Automated External Defibrillators recalled by Defibtech | Defibtech | Other | Nationwide |
| Device | CLASS II | Automated External Defibrillators recalled by Defibtech | Defibtech | Other | CT |
| Device | CLASS II | Automated External Defibrillators recalled by Defibtech | Defibtech | Other | Nationwide |
| Device | CLASS II | Automated External Defibrillators recalled by Defibtech | Defibtech | Other | Nationwide |
| Device | CLASS II | Semi-Automated External Defibrillators recalled by Defibtech | Defibtech | Other | Nationwide |
| Device | CLASS II | DDP-2002: Pediatric Defibrillation Pads For use with AED recalled | Defibtech | Lead & Heavy Metals | CT |
All defibtech recalls, newest first
14 totalAbout this list
Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.