All recall categories

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.

3,078 stored notices name Connecticut, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,759 notices were distributed nationwide, so they reach Connecticut too — those are in the archive.

Food

Reported Feb 5, 2025

Alpha Test 120 count Black labeled plastic bottle, 12 bottles per case of 120 count capsules each per bottle, Store in…

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

Iovate Health Sciences USA Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Feb 5, 2025

Brand Name: SenTiva" Product Name: VNS Therapy" SenTiva", Model 1000 Model/Catalog Number: 1000 Software Version: NA…

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

LivaNova USA, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 5, 2025

Medtronic PIN, 100mm STERILE PERCUTANEOUS REF: 9733235 Medtronic PIN, 150MM, STERILE PERCUTANEOUS REF: 97733236 The…

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

Medtronic Navigation, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 29, 2025

BD PCR Cartridges used with MAX System. Model Number: 437519

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

Becton Dickinson & Co.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 29, 2025

Merlin.net Patient Care Network (PCN) Heart Failure Web Application (Model MN6000) (Which interfaces with CardioMEMS"…

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

St. Jude Medical

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Jan 29, 2025

The Granola Bar brand The OG Bar; 4 oz; Ingredients: Oats, brown sugar, honey, almonds, butter, olive oil, cashews,…

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

The Granola Bar

FDA (openFDA food enforcement)

Medical devices

Reported Jan 22, 2025

McKesson Cardiology Hemo software

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

A L I Technologies Ltd.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 22, 2025

Brand Name: Alcon Product Name: Monarch¿ III D Delivery Cartridge Model/Catalog Number: 8065977763 Product Description:…

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

Alcon Research LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 22, 2025

Panther Fusion GBS Assay REF PRD-04484 Kit containing Panther Fusion GBS Reagent Cartridge IVD.

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

Hologic, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 22, 2025

8MM, MONOPOLAR CURVED SCISSORS, IS4000 REF 470179

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

Intuitive Surgical, Inc.

38 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 22, 2025

Karl Storz - Endoskope - REF 723400 - Optical Biopsy and Grasping Forceps, CE

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

Karl Storz Endoscopy

FDA (openFDA device enforcement)

Medical devices

Reported Jan 22, 2025

Neo-Tee T-Piece Resuscitator, for pediatric emergency respiratory support, Part: 1050805, 1050808, 1050809, 1050810,…

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

Mercury Enterprises, Inc. dba Mercury Medical

FDA (openFDA device enforcement)

Food

Reported Jan 22, 2025

Yu Yee, Five Spice Powder,1.76oz

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

Summit Import Corporation

FDA (openFDA food enforcement)

Medical devices

Reported Jan 15, 2025

AMT Mini Enteral Extension Set, 12" Right Angle Feeding Set with Y-Port. Model/Catalog Number: E6-1222

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

Applied Medical Technology Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 15, 2025

EnVisio Patient Pad Transition Cushion, Model/Catalog Number: ENVISIO-SYS Product Description: The EnVisio Patient Pad…

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

Elucent Medical Inc.

FDA (openFDA device enforcement)

Food

Reported Jan 15, 2025

WELLSLEY FARM VANILLA NON-FAT GREEK YOGURT; 40 oz; UPC 888670048078

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

HP Hood (VERNON)

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Jan 15, 2025

Olympia Foods Grecian Dip Tzatziki sauce, item 100, 4 lb. tubs, UPC 10045059001001, 4 tubs per case; item 104, 32lbs…

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

Olympia Foods

FDA (openFDA food enforcement)

Medical devices

Reported Jan 15, 2025

Xhibit Telemetry Receiver, Model 96280, with Service Manual. Intended to provide monitoring system with patient data.

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

Spacelabs Healthcare, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jan 8, 2025

3M Unitek Transbond Plus Self-Etching Primer REF 712-090 (100 unit box) 712-091 (20 unit box) Transbond Plus Self…

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

3M Unitek Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Jan 8, 2025

AURYON LASER SYSTEM 100-120 VAC. Model Number: EXM001. Product Number: EXM-2001-1100

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

Angiodynamics, Inc.

FDA (openFDA device enforcement)

Food

Reported Jan 8, 2025

a.) King Kullen brand Vegetable Platter; UPC 85316-10005; 44oz plastic container b.) Wild by Nature brand Vegetable…

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

Gracie's Kitchens Inc.

33 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Jan 8, 2025

--- Organic Baby Carrots --- Organic Baby Peeled Carrots 12/12oz Steam-to-Serve; Organic Baby Peel Carrot12/12oz…

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

Grimmway Enterprises, Inc. dba Grimmway Farms

4 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jan 1, 2025

The Merlin PCS 3650 programmer Model 3330 The Merlin PCS programmer model 3650 is a portable, dedicated programming…

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

Abbott Medical

FDA (openFDA device enforcement)

Medical devices

Reported Jan 1, 2025

20/30 INDEFLATOR, REF: 1000184, for use during cardiovascular procedures in conjunction with interventional devices…

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

Abbott Vascular Inc.

3 more products in this recall

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.