Reported Jun 24, 2020 · Terminated

DDU-2300 Lifeline/ReviveR View, Model Numbers DDU-C2300EN, DDU-C2300CA, DDU-A2300EN, DDU-E2300EN Catalog Numbers…

Defibtech, LLC

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Defibtech, LLC · 741 Boston Post Rd · Guilford, CT · 06437-2714

Is this the product you have?

  • DDU-2300 Lifeline/ReviveR View, Model Numbers DDU-C2300EN, DDU-C2300CA, DDU-A2300EN, DDU-E2300EN Catalog Numbers
    • CCD-A1006RX
    • CCD-A1013EN
    • CCD-A1015EN
    • DCF-A2310EN
    • DCF-A2310RX
    • DCF-A2313EN
    • DCF-C2310CA
    • DCF-C2310EN
    • DCF-E2310CA
    • DCF-E2310EN
    UDI 00815098020201, 00815098020225, 00815098020232
  • Product UsageAutomated External Defibrillators (AED) are indicated for use on victims
  • of sudden cardiac arrest (SCA) who are- unconscious and unresponsive, not breathing or not breathing normally
Lot codes and dates
  • Serial Numbers

    765 of 765 codes

    • 400086354
    • 400086358
    • 400090005
    • 400091761
    • 400093477
    • 400093478
    • 400093479
    • 400093480
    • 400093481
    • 400093482
    • 400093483
    • 400093484
    • 400093485
    • 400093486
    • 400093487
    • 400093488
    • 400093489
    • 400093490
    • 400093491
    • 400093492
    • 400093493
    • 400093494
    • 400093495
    • 400093496
    • 400093497
    • 400093498
    • 400093499
    • 400093500
    • 400093501
    • 400093502
    • 400093503
    • 400093504
    • 400093505
    • 400093506
    • 400093508
    • 400093510
    • 400093512
    • 400093513
    • 400093514
    • 400093515
    • 400093516
    • 400093517
    • 400093518
    • 400093519
    • 400093520
    • 400093521
    • 400093522
    • 400093523
    • 400093524
    • 400093525
    • 400093527
    • 400093528
    • 400093529
    • 400093530
    • 400093531
    • 400093532
    • 400093533
    • 400093534
    • 400093535
    • 400093536
Amount recalled
860

This recall covers 3 products

The agency filed one notice per product. You are reading one of them; the other 2 are below.

Where it was sold

  • Nationwide

Why it was recalled

A component issue may cause the AED to abort a shock delivery or reset unexpectedly, which may cause an affected device to fail to delivery shock, and/or to fail to deliver shock in range.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

Free recall alerts

Get alerted about new Defibtech, LLC recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Jan 8, 2021 · Data as of Sep 19, 5:31 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.