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U.S. Department of Health and Human Services

Class 2 Device Recall Lifeline View

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 Class 2 Device Recall Lifeline Viewsee related information
Date Initiated by FirmMarch 18, 2025
Date PostedApril 29, 2025
Recall Status1 Open3, Classified
Recall NumberZ-1692-2025
Recall Event ID 96618
PMA NumberP160032 
Product Classification Automated external defibrillators (non-wearable) - Product Code MKJ
ProductAutomated External Defibrillators, Model DDU-2300. Item numbers: DCF-E2310D3/1(German/English dual language), DCF-E2310E3/1(German/French dual language), DCF-E2310F3/1 (French/English dual language), DCF-E2310G3/1(French/German dual language), DCF-E2310IT (Italian language)
Code Information UDI-DIs: 00815098020232 (DDU-2300, export version), 10815098020239 (DDU-2300, export version (configuration level)). Lot numbers: 400174411, 400174755, 400175965, 400179100, 400179205, 400179279, 400179223, 400179206, 400179271, 400191481, 400191516, 400197352, 400191375, 400164982, 400155836, 400159075, 400139521, 400168419, 400160156, 400165319, 400190176, 400187549, 400187582, 400190198, 400186761, 400187569, 400150859, 400150811, 400187620, 400150948, 400182206, 400152805, 400200222, 400173689, 400173695, 400170424, 400182464, 400191479, 400179417, 400179733, 400168929, 400179607, 400179275, 400191478, 400151695, 400151696, 400151699, 400151718, 400151724, 400151727, 400151728, 400151730, 400151756, 400151799, 400151802, 400151812, 400151841, 400151843, 400151844, 400151858, 400151905, 400151907, 400151915, 400151920, 400156160, 400186774, 400187567, 400187593, 400187596, 400190090, 400190232, 400190280, 400190303, 400190304, 400190305, 400190318, 400190322, 400190324, 400190355, 400151697, 400151723, 400151851, 400151852, 400151916, 400154576, 400154581, 400154589, 400154595, 400154601, 400154645, 400154646, 400154698, 400154755, 400154839, 400157339, 400157485, 400157486, 400157489, 400157490, 400157510, 400157512, 400157514, 400157516, 400157521, 400150824, 400150860, 400150932, 400141200, 400141209, 400141210, 400141239, 400141257, 400141260, 400141266, 400141275, 400148165, 400148173, 400148186, 400148208, 400148213, 400148247, 400148275, 400150548, 400150839, 400150846, 400150847, 400150848, 400150873, 400150888, 400150894, 400150899, 400150903, 400150912, 400150915, 400150916, 400150921, 400150930, 400150933, 400150936, 400150937, 400150958, 400150959, 400150962, 400150965, 400150968, 400150969, 400150979, 400150991, 400156277, 400156418, 400156430, 400156431, 400187368, 400187561, 400187579, 400187601, 400190175, 400150825, 400150892, 400150911, 400150964, 400187539, 400187583, 400190295, 400187697, 400187703, 400187704, 400187708, 400187719, 400187730, 400187747, 400190293, 400190365, 400190366, 400190381, 400190412, 400190415, 400081869, 400081970, 400170423, 400173514, 400154604, 400154608, 400154609, 400154613, 400154666, 400154671, 400154684, 400154798, 400154799, 400154810, 400168739, 400168745, 400168809, 400168926, 400168943, 400168951, 400168997, 400172421, 400173420, 400173433, 400173489, 400173496, 400173509, 400173513, 400173539, 400173540, 400159593, 400159613, 400162216, 400162221, 400162248.
FEI Number 3003521780
Recalling Firm/
Manufacturer		 Defibtech, LLC
741 Boston Post Rd Ste 201
Guilford CT 06437-2714
For Additional Information ContactDefibtech Customer Service
203-453-6654
Manufacturer Reason
for Recall		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).
FDA Determined
Cause 2		Process control
ActionOn March 18, 2025 URGENT FIELD SAFETY NOTICE letters were emailed to customers. Actions to be taken by the Customer/User: 1. Confirm receipt of this notice by replying to this email with RECEIVED 2. Please complete the attached Customer Reply Form and email the form to FA2025- 02@defibtech.com. 3. Attached to this Field Safety Notice, you will find the 3 Instructions For Use (Operator Guide) in the required languages. Please take the attached 3 Instructions For Use (Operator Guide) and keep with the affected AED(s). If you have questions now, please feel free to contact us using the email address: FA2025-01@defibtech.com. Defibtech is committed to ensuring our products meet the highest quality standards and that our customers are fully supported. I sincerely apologize for any inconvenience this may cause you. As always, Defibtech Customer Support is available by calling 1-877-453-4507, 7:30 A.M. to 6:00 P.M. (Eastern), Monday - Friday. Thank you for your attention and cooperation.
Quantity in Commerce212 units (OUS only)
DistributionInternational Only: Switzerland.
Total Product Life CycleTPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 The manufacturer has initiated the recall and not all products have been corrected or removed. This record will be updated as the status changes.
PMA DatabasePMAs with Product Code = MKJ
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