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Recalls distributed in Connecticut

These notices name Connecticut in the distribution list the company gave its agency. That list says where the product was shipped, not where it ended up — a recalled item can travel with a shopper, and some notices list no states at all.

3,041 stored notices name Connecticut, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Connecticut too — those are in the archive.

Medical devices

Reported May 27, 2026

Swan-Ganz Catheter, Models: 131F7/131F7P, 131F7J, 141F7, 151F7, 834F75, 096F6/096F6P, C144F7, 782F75M, 132F5, C146F7,…

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

Becton, Dickinson and Company

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 27, 2026

Silastic Foley Catheters Silastic Brand Foley Catheter 30cc REF: 33416 33418 33420 33422 33424 Silastic Brand Foley…

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

C.R. Bard Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 27, 2026

Oncology Kit w/60" (152 cm) Appx 2.2 ml, Smallbore Ext Set w/ChemoLock Port, Clamp, Anti-Siphon Valve, Spiros;…

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

ICU Medical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 27, 2026

OneLIF Interbody Cage (REF/Description): 010-107-1007/Small 7 Degree 10mm X 7mm, 010-107-1007-2/Small 7 Degree 10mm X…

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

Novapproach Spine, LLC

FDA (openFDA device enforcement)

Medical devices

Reported May 20, 2026

Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name: Dexcom G7 CGM iOS App Model/Catalog Number:…

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

Dexcom, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 20, 2026

Edwards EVOQUE tricuspid delivery system REF:9850TDS Sterile EO

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

Edwards Lifesciences, LLC

FDA (openFDA device enforcement)

Medical devices

Reported May 20, 2026

Codman CerebroFlo EVD Catheter with Endexo Technology. Contains 5 sets. Product ID: 37.550.501. The CerebroFlo EVD…

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

Integra LifeSciences Corp. (NeuroSciences)

FDA (openFDA device enforcement)

Food

Reported May 20, 2026

Prospector Popcorn brand Belgian Chocolate Toffee flavored popcorn; Ingredients: Non-GMO popcorn, brown sugar, corn…

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

Prospector Popcorn, LLC

FDA (openFDA food enforcement)

Food

Reported May 20, 2026

Swad Orange Flavored Masala Candy

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

Raja Foods and Vegetables Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported May 13, 2026

ERBEFLO CleverCap CO2: Hybrid CO2 Tubing/Cap Set for Olympus Scopes & CO2 Sources, REF: 20325-239; Hybrid CO2…

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

Erbe Medical, LLC

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported May 13, 2026

french broad CHOCOLATE bette's bake sale (a multi-flavor bonbon assortment). 6-piece NET WT. 2.5 OZ (70.75G); 12-piece…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

French Broad Chocolate Factory

FDA (openFDA food enforcement)

Medical devices

Reported May 13, 2026

Intuitive 8 mm SureForm 30 Gray Reloads Reference Numbers: 48230M-05 and 48230M-06

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Intuitive Surgical, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported May 13, 2026

LUNDBERG FAMILY FAMRS WHITE RICE JASMINE NET WT 32 OZ (2 lb) 907 g Manufactured and Distributed by: Lundberg Family…

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

Wehah Farms

FDA (openFDA food enforcement)

Medical devices

Reported May 6, 2026

Brand Name: HiResolution" Bionic Ear System Product Name: M Zn-Air Battery Pak Model/Catalog Number: CI-5501-110;…

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

Advanced Bionics, LLC

FDA (openFDA device enforcement)

Medical devices

Reported May 6, 2026

Brand Name: Kiwi Omni Vacuum Delivery System Product Name: Kiwi Omni Vacuum Delivery System Model/Catalog Number:…

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

Clinical Innovations, LLC

FDA (openFDA device enforcement)

Food

Reported May 6, 2026

Negita Cracker- Shrimp 2.8oz

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

Hadson (Toko) Trading Co. Inc.

FDA (openFDA food enforcement)

Medical devices

Reported May 6, 2026

Immy, Myco DDR Trident, Bulk Neutralization Buffer B (60 X 30 mL), REF: TBPN67-60 For processing of clinical specimens…

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

Immuno-Mycologics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 29, 2026

nanOss 3D Advanced Bone Graft Substitute nanOss 3D Plus Advanced Bone Graft Substitute 90-300-251008: nanOss 3D…

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

XTANT Medical Holdings, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 22, 2026

iLet Ace Pump Kit REF: BB1001 iLet Dosing Decision Software

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

Beta Bionics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 22, 2026

Instinct Plus Endoscopic Clipping Device REF: G58010 Rx Only, Sterile EO

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

Wilson-Cook Medical Inc.

FDA (openFDA device enforcement)

Food

Reported Apr 15, 2026

Vital Nutrients Aller-C (vitamin C, citrus bioflavonoids, isoquercitrin, and bromelain)100 count bottles and 200 count…

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

Blueroot Health, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 15, 2026

B¿R¿A¿H¿M¿S KRYPTOR compact REACT, REF: 89986, used with B¿R¿A¿H¿M¿S PlGF Plus KRYPTOR, REF: 859075N, and run on the…

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

Brahms GmbH

FDA (openFDA device enforcement)

Medical devices

Reported Apr 15, 2026

Stryker Sustainability Solution Color Cuff 24" (Yellow) Quick Connect Dual Port Single Bladder REF 5921-024-235 Stryker…

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

Stryker Sustainability Solutions

FDA (openFDA device enforcement)

Medical devices

Reported Apr 15, 2026

Tornier HRS Max parts: 1. TORNIER HRS Max Tuberosity Body Lat Coat, Small, Cat. No. ARS1041101 2. TORNIER HRS Max…

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

Tornier, Inc.

FDA (openFDA device enforcement)

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Other states

RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.