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Recall Observatory FDA recall evidence

Device product

Automated External Defibrillators, Model DDU-2200, IItem numbers: DCF-E2210-D3/1¿(German/English dual language), DCF-E2210-F3/1¿(French/English dual language)

Z-1694-2025

March 18, 2025

Class II

Product summary

Firm
Defibtech, LLC
Event
Event 96653
Status
Ongoing
Classification
Class II
Quantity
13 units (OUS only)
Official record key
device-enforcement:Z-1694-2025

Official wording

Reason: It was noticed there was no Italian translation included for the AED. Article 16 of the Swiss Medical Devices Ordinance (MedDO) states that product information (labelling and instructions for use) should be provided in all three official languages of Switzerland (German, French, and Italian).

Code information: UDI-DIs; 00815098020195 (DDU-2200, export version), 10815098020192 (DDU-2200, export version (configuration level)); Lot numbers: 400184748, 400170814, 400180780, 400142381, 400142390, 400142995, 400145936, 400145955, 400149039, 400149042, 400149094, 400145977, 400149090,

Distribution pattern: OUS only: Switzerland.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    It was noticed there was no Italian translation included for the AED. Article 16 of the Swiss Medical Devices Ordinance (MedDO) states that product information (labelling and instructions for use) should be provided in all three official languages of Switzerland (German, French, and Italian).