🔔 Product Recalls & Refunds in Connecticut

5 active product recalls & refunds in connecticut — verified and updated daily.

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Product Recalls & Refunds in Connecticut (5 active)
Defibtech, LLC: Defibtech DDP-2002: Pediatric Defibrillation Pads For use with AED Models: Lifeline View Auto, lifeline Pro, Lifeline ECG, Lifeline View (DDU-2XXX Series -Indicated for use on victims of sudden cardiac arrest (SCA.) FDA device recall — free correction, repair, or replacement from manufacturer or authorized retailer

Recall reason: Within the Irish Market, that a Field Safety Notice is being issued due to a select number of authorized labelled Defibtech AED Pads, which have

Product Recall CT
Defibtech, LLC: Defibtech DDP-100 Adult Defibrillation Pads For use with AED Models: Lifeline and Lifeline Auto (DDU-1:XX Series)- Indicated for use on victims of sudden cardiac arrest (SCA) FDA device recall — free correction, repair, or replacement from manufacturer or authorized retailer

Recall reason: Within the Irish Market, a Field Safety Notice is being issued due to a select number of authorized labelled Defibtech AED Pads, which have had t…

Product Recall CT
Defibtech, LLC: Defibtech DDP-200P: Pediatric Defibrillation Pads 0 For use with AED Models: Lifeline and Lifeline Auto (DDU-l XX Series)-Indicated for use on victims of sudden cardiac arrest (SCA.) FDA device recall — free correction, repair, or replacement from manufacturer or authorized retailer

Recall reason: Within the Irish Market, that a Field Safety Notice is being issued due to a select number of authorized labelled Defibtech AED Pads, which have

Product Recall CT
Defibtech, LLC: Defibtech DDP-2001: Adult Defibrillation Pads For use with AED Models: Lifeline View Auto, lifeline Pro, lifeline ECG, lifeline View (DDU-2XXX Series). -Indicated for use on victims of sudden cardiac arrest (SCA.) FDA device recall — free correction, repair, or replacement from manufacturer or authorized retailer

Recall reason: Within the Irish Market, that a Field Safety Notice is being issued due to a select number of authorized labelled Defibtech AED Pads, which have

Product Recall CT
Prospector Popcorn, LLC: Prospector Popcorn brand Belgian Chocolate Toffee flavored popcorn; Ingredients: Non-GMO popcorn, brown sugar, corn syrup, butter, vanilla, baking soda, sea salt, white chocolate (sugar, palm kernel fat, skimmed milk powder [ FDA food recall — return recalled product to store for a full refund of purchase price

Recall reason: Products contain undeclared soy, specifically soy lecithin.. Recalled by Prospector Popcorn, LLC. Distribution: CT and NY. Classification (Class

Product Recall CT

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