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.

3,041 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.

Food

Reported May 6, 2020

5.5 oz cans of Ocean Spray Pink Lite Cranberry Juice Drink

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

Ocean Spray Cranberries Inc.

FDA (openFDA food enforcement)

Medical devices

Reported May 6, 2020

Lead diagnostic electrocardiograph under the following device names: ELI 10, ELI 350, ELI 150c, ELI 250c, ELI 230, ELI…

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

Welch Allyn, Inc/mortara

9 more products in this recall

FDA (openFDA device enforcement)

Food

Reported May 6, 2020

Whole Foods Market Minestrone Soup PLU code printed on the product scale labels beginning with 248529 for soup sold in…

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

Whole Foods Market

FDA (openFDA food enforcement)

Medical devices

Reported Apr 29, 2020

ARCHITECT HAVAB G Reagent Kit. List Number 6L27 25.

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

Abbott GmbH & Co. KG

FDA (openFDA device enforcement)

Medical devices

Reported Apr 29, 2020

TCM4 Base unit, Ref 391-880, UDI:(01)05700693918808, used with the monitor modules TCM4 (902-778), TCM40 (902-778,…

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

Radiometer Medical ApS

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 22, 2020

The CF-70 instrument (product code: LXG; Regulation Number: 862.2050) receives magazines containing stained blood…

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

Sysmex America, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 15, 2020

ARCHITECT C System Mixer - Product Usage: The ARCHITECT Clinical Chemistry System is designed to perform automated…

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

Abbott Laboratories, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 15, 2020

GEM Microvascular Anastomotic Coupler Devices - Product Usage: is intended to be used in the anastomosis of veins and…

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

Baxter Healthcare Corporation

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 15, 2020

BIOMET StageOne Hip Cement Spacer Mold with Insert, 48 MM, Silicone, Sterile, Item 431181.

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

Biomet, Inc.

32 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 15, 2020

Firefly Floorsitter, Firefly Splashy Bathseat, Firefly GoTo Seat - Product Usage: The Splashy Bath-Seat is a Portable…

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

James Leckey Design Ltd.

FDA (openFDA device enforcement)

Food

Reported Apr 15, 2020

Lindt & Sprungli (USA), Inc.; Excellence 85% Cocoa Dark Chocolate; Net WT 3.5OZ (100g)

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

Lindt & Sprungli (USA), Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 15, 2020

ABL800 FLEX, model number/UDI 393-800/0570 In Vitro testing of samples of whole blood for the parameters pH, pO2, pCO2,…

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

Radiometer Medical ApS

FDA (openFDA device enforcement)

Food

Reported Apr 15, 2020

Whole Foods Vodka Sauce, 6-16 oz. containers.

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

Winter Gardens Quality Foods, Inc.

FDA (openFDA food enforcement)

Food

Reported Apr 8, 2020

Sushi Ebi Cooked Butterfly Tail-On Whiteleg Shrimp; Tray +0.498 pounds; 20 individual trays per case Distributed by AFC…

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

Advanced Fresh Concepts Corp.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 8, 2020

Avalon Elite Vascular Access Kit, Model No. 70106.3540, UDI 04037691831039

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

Maquet Cardiovascular US Sales, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2020

Merits E604 Pilot Navigator Stairlift - Product Usage: To transport patients up stairs.

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

Merits Holdings Co. dba Merits Health Products, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2020

Philips V60 Ventilators with Power Management PCBA part number 1055906

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

Respironics California, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2020

NAVIO Soft Tissue Protector, included in instrument kits. The NAVIO Tissue Protector is a reusable instrument designed…

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

Smith & Nephew, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2020

Instructions for Use and Surgical Cleaning and Sterilization Protocol for: (1) Trilliant Surgical Tiger Cannulated…

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

Trilliant Surgical, LLC

10 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 1, 2020

Precision Xtra Blood Glucose & Ketone Monitoring System, UDI: 00093815715023, 00093815988144

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

Abbott Diabetes Care, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Apr 1, 2020

Raisins packed in following brand names and sizes: 6 pack cartons (6 X 1 oz. boxes) - Pickwell Farms, Southern Grove,…

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

Caruthers Raisin Packing Co., Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 1, 2020

Intellijoint Navigation System, Software Application, IJK1 (P/N 000-0547) - Product Usage: The Intellijoint Navigation…

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

Intellijoint Surgical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 1, 2020

Karl Storz NEURO-FIBERSCOPE, Model # 11282BN1, Flexible Pediatric Neuroscope

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

Karl Storz Endoscopy

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 1, 2020

VNS Therapy Programmer, Model 3000 used with Models 103, 104, 105, 106, or 8103 VNS Therapy generators.

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

LivaNova USA 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.