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.

Medical devices

Reported Oct 13, 2021

Access hsTnI High Sensitivity Troponin I, REF B52699 Access Immunoassay System REAGENT PACK

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

Beckman Coulter Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 13, 2021

CardioQuip, Modular Cooler-Heater, Model: MCH-1000(i), CE 2797, UDI: (01)00860000846103

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

CardioQuip, LLC

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 13, 2021

Nutrifill Scleral, Hybrid, and Gas Permeable (GP) Lens Insertion Solution, Physiologic Formula, Preservative Free, 35…

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

Contamac Solutions, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 13, 2021

GEL CONDUCTOR, Description/REF: 5 LITER W/DISP/4238, 24-8.5OZ BOTTLES/4248, 5 LITER/4266, distributed by DJO, LLC / DJO…

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

Djo, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 13, 2021

Flower E-Kit, Advanced-Bone Fixation Fasterner-Fixation of Ref: EWK 201

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

Flower Orthopedics Corporation

FDA (openFDA device enforcement)

Food

Reported Oct 13, 2021

Mr. Nut brand Dried Oleaster Net Wt: 10.6 OZ (300g). Expiration date 10/2022. UPC 0360894900.

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Vintage Food Corp.

FDA (openFDA food enforcement)

Medical devices

Reported Oct 6, 2021

VACUETTE TUBE 6 ml K2E K2EDTA 13x100 pink cap-pink ring, non-ridged

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

Greiner Bio-One North America, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 6, 2021

Covidien HysteroLux Fluid Management System Control Unit, REF: 72205000

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

WOM World

FDA (openFDA device enforcement)

Medical devices

Reported Sep 29, 2021

Greiner Bio-One VACUETTE¿ TUBE 2 ml 9NC Coagulation sodium citrate 3.2% 13x75 blue cap-white ring, sandwich tube,…

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

Greiner Bio-One North America, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 29, 2021

CoLink Bone Graft Harvester, 8mm, Sterile, Disposable, REF G05 S1008 - Product Usage: is a general instrument intended…

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

In2bones USA, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Sep 29, 2021

EPIQ Diagnostic Ultrasound Systems: Software Versions 5.0, 5.0.1 and 5.0.2 Models: EPIQ 5 - 795120 EPIQ 5C - 795205…

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

Philips Ultrasound Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 22, 2021

Trader Joe's Nuts Raw California Walnut Baking Pieces NET WT. 16 OZ (1 LB) 454g SKU# 51934-89685 UPC 0051 9342 Contains…

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

Andersen & Sons Shelling, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Sep 22, 2021

BD Extension Set SMALLBORE Tubing with 2 SmartSite VALVES, REF: 20019E

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

Carefusion

14 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 22, 2021

Arjo Disposable Repositioning Sling, Model AHD001

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

Getinge Dominican Republic SA

FDA (openFDA device enforcement)

Food

Reported Sep 15, 2021

Fermentation Derived Pepsin Product packaging: 5 individual LDPE bags with a net weight of 5kg each and 2.5kg sample…

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

Ingredion

FDA (openFDA food enforcement)

Food

Reported Sep 15, 2021

Banoful Top Orange Biscuit

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

Kbf Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Sep 15, 2021

Pipeline Flex Embolization Device

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

Micro Therapeutics Inc.,

1 more product in this recall

FDA (openFDA device enforcement)

Drugs

Reported Sep 15, 2021

QiYu Hand Sanitizer (ethyl alcohol 75% (v/v)), 16.9 FL OZ (500 ML) bottles, Manufactured by: Guangzhou Minghui…

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

Native Promotions, Inc.

FDA (openFDA drug enforcement)

Medical devices

Reported Sep 8, 2021

CareStart COVID-19 Antigen Rapid Diagnostic Test for the detection of SARS-CoV-2 Antigen Qualitative detection of the…

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

Versea Diagnostics LLC

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 8, 2021

CoolSculpting Elite System The CoolSculpting System SW release 2.0, SW release 3.0, SW release 3.0.1, SW release 3.0.2

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

Zeltiq Aesthetics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 1, 2021

BD" Mouse IgG2a Isotype Control APC X39 ASR

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

Becton, Dickinson and Company, BD Biosciences

FDA (openFDA device enforcement)

Medical devices

Reported Sep 1, 2021

Monoject 0.9% Sodium Chloride Flush Syringe, 10 mL Fill, STERILE, Product Code 8881570121 The proposed device is…

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

Cardinal Health

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 1, 2021

NES Reprocessed Visions PV .035 IVUS Catheter, Sterile. For use in the evaluation of vascular morphology in blood…

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

Northeast Scientific Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 25, 2021

OPTI SARS-CoV-2 RT-PCR Test, REF Numbers: a) 99-57003 b) 99-57004

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

OPTI Medical Systems, 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.