Medical device makerLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field. in United StatesLabelled by claude-haiku-5.5 from the firm's FDA names. It is not an FDA field.. FDA records under 2 spellings of its name, each linked to the record.
As of Nov 14, 2026, FDA's public records list Defibtech with 14 device recalls and 9 510(k) clearances. The most recent is a device recall dated Mar 18, 2025: Semi-Automated External Defibrillators; Models: DDU-100 and DDU-100E. Item numbers: DCF-….
Drug approvals, 510(k) clearances, recalls and letters, 2017 to 2026 to date
A hatched bar is a year that is not over, so its count covers only part of the year.
| Mar 18, 2025 | Semi-Automated External Defibrillators; Models: DDU-100 and DDU-100E. Item numbers: DCF-E110SG-DE/1 (German language), DCF-E110SG-FR/1 (FrenClass II · It was noticed there was no Italian translation included for the AED. Article 16 of the Swiss Medical Devices Ordinance | Device recalls |
| Mar 18, 2025 | Automated External Defibrillators, Model DDU-2200, IItem numbers: DCF-E2210-D3/1¿(German/English dual language), DCF-E2210-F3/1¿(French/EnglClass II · It was noticed there was no Italian translation included for the AED. Article 16 of the Swiss Medical Devices Ordinance | Device recalls |
| Mar 18, 2025 | Automated External Defibrillators, Model DDU-2450. Item number: DCF-E2460DE (German language)Class II · It was noticed there was no Italian translation included for the AED. Article 16 of the Swiss Medical Devices Ordinance | Device recalls |
| Mar 18, 2025 | Automated External Defibrillators, Model DDU-2200, IItem numbers: DCF-E2210-D3/1¿(German/English dual language), DCF-E2210-F3/1¿(French/EnglClass II · It was noticed there was no Italian translation included for the AED. Article 16 of the Swiss Medical Devices Ordinance | Device recalls |
| Mar 18, 2025 | Automated External Defibrillators, Model DDU-2300. Item numbers: DCF-E2310D3/1¿(German/English dual language), DCF-E2310E3/1¿(German/French Class II · It was noticed there was no Italian translation included for the AED. Article 16 of the Swiss Medical Devices Ordinance | Device recalls |
| Oct 14, 2024 | Defibtech DDP-2001: Adult Defibrillation Pads For use with AED Models: Lifeline View Auto, lifeline Pro, lifeline ECG, lifeline View (DDU-2Class II · Within the Irish Market, that a Field Safety Notice is being issued due to a select number of authorized labelled Defibt | Device recalls |
| Oct 14, 2024 | Defibtech DDP-200P: Pediatric Defibrillation Pads 0 For use with AED Models: Lifeline and Lifeline Auto (DDU-l XX Series)-Indicated for useClass II · Within the Irish Market, that a Field Safety Notice is being issued due to a select number of authorized labelled Defibt | Device recalls |
| Oct 14, 2024 | Defibtech DDP-100 Adult Defibrillation Pads For use with AED Models: Lifeline and Lifeline Auto (DDU-1:XX Series)- Indicated for use on vicClass II · Within the Irish Market, a Field Safety Notice is being issued due to a select number of authorized labelled Defibtech A | Device recalls |
Spellings are joined only when they reduce to the same name, or a reviewed source names the same company. Sharing an FDA establishment number (FEI) is not enough: contract sites make products for many firms. Facts marked AI were labelled by a language model from the firm's FDA names; everything else comes from FDA or Wikidata. How this page is built
