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.
Reported Dec 27, 2023
AC Power Adapter for use with the LIFEPAK 15 Monitor/Defibrillator, REF: 11140-000098
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Physio-Control, Inc.
FDA (openFDA device enforcement)
Reported Dec 20, 2023
Deli Express, Deli Club 4.4oz wedge sandwich, 10 retail units per wholesale case, UPC 41433-00157
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.E.A. Sween Co.
FDA (openFDA food enforcement)
Reported Dec 20, 2023
Acorn Raspberry Creme Filled Cookie found in gift basket: #067 Believe Cookie, Cake and Brownie Collection
High riskUsing this product could cause serious injury, illness or death — stop using it now.Houdini Inc.
8 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 20, 2023
CereLink ICP Extension Cable (Extension Cable), Model No. 826845 Used with Codman CereLink Intracranial Pressure (ICP)…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Integra LifeSciences Corp.
FDA (openFDA device enforcement)
Reported Dec 20, 2023
STERILE PVP SOLUTION, REF DYNDA1907
Moderate riskThis product could cause temporary or reversible health problems — stop using it.MEDLINE INDUSTRIES, LP - Northfield
9 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 13, 2023
Monarch Platform REF MON-000005-01, 100-240V- 50/60Hz 1440w
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Auris Health Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 13, 2023
BIOFIRE Blood Culture Identification 2 (BCID2) Panel, REF: RFIT-ASY-0147, used with Maine Molecular Quality Controls,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
FDA (openFDA device enforcement)
Reported Dec 13, 2023
CardioQuip Modular Cooler-Heater, Model:MCH-1000(m), Power: 115V-60hz,16A
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CardioQuip, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 13, 2023
Hans Kissle Potato Salad White Homestyle, 10 lb. bulk case, UPC Codes: 00036217701003
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hans Kissle Company, LLC
FDA (openFDA food enforcement)
Reported Dec 13, 2023
Freedom Boom models series: F110, F120, F130, F320, F330, F350, F410, and F420 with built in 42A Lightweight Spring Arm…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ihb Operations B.v.
FDA (openFDA device enforcement)
Reported Dec 13, 2023
Multi-Mode Stimulator, Transcutaneous Electrical Nerve Stimulation
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Liberty Medical Solutions, LLC
FDA (openFDA device enforcement)
Reported Dec 13, 2023
EVO+VISIAN Implantable Collamer Lens, REF:VICM5_12.1. Phakic Intraocular lens.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Staar Surgical Company
10 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 13, 2023
Vermont Village Organic Unsweetened Apple Sauce (24oz); UPC 362401 | 084648311285
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stonewall Kitchen, LLC
FDA (openFDA food enforcement)
Reported Dec 13, 2023
NovoTHOR Gen 2.0 whole body red light therapy bed, model S1176
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Thor Photomedicine Ltd.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 6, 2023
Acumen IQ Sensor, REFs: AIQS6, AIQS65, AIQS6R, AIQS6R5, AIQS8, AIQS85, AIQS8R5, Rx only, Sterile EO. For use in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Edwards Lifesciences, LLC
5 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 6, 2023
Breakfast Sandwich Bacon Egg & Cheddar Croissant Net Wt. 5.25oz (149g) UPC:766375253051. Packaged in clamshell…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Coastal Companies dba Hearn Kirkwood
4 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 29, 2023
BD Alaris Pump infusion sets (Product Name, Catalog #) BD AlarisTM Pump Infusion Set Vented syringe adapter Smallbore…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Company
2 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 29, 2023
FilmArray TORCH REF HTFA-ASY-0104. HTFA-ASY-0104 is the BIOFIRE TORCH Base which includes barcode scanner, touch screen…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
FDA (openFDA device enforcement)
Reported Nov 29, 2023
EXALT Model D Single-Use Duodenoscope: Outer box UPN# M00542420 & Outer box UPN# M0054242CE0.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 29, 2023
Solea Models 2.0 and 3.0 Laser Surgical Instrument, Foot Pedal assembly SUB-00434 with foot pedal CUS-00226 Rev. K…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Convergent Dental
FDA (openFDA device enforcement)
Reported Nov 29, 2023
Ventlab, LLC AirFlow manual resuscitator devices with integrated manometer, multiple accessory configurations to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.SunMed Holdings, LLC
8 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 19, 2023
Skyline Provisions, Inc. Recalls Raw Ground Beef Products Due to Possible Foreign Matter Contamination
High riskUsing this product could cause serious injury, illness or death — stop using it now.Skyline Provisions
USDA FSIS
Reported Nov 15, 2023
Similac Probiotic Tri-Blend - 0.017oz (0.50g) packaged in foil packets. 50 foil packets per carton - 3 cartons per case.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Laboratories
FDA (openFDA food enforcement)
Reported Nov 15, 2023
BREG REF 100519-000 WALKER FOLDING WALKER WITH WHEELS Utilized as a walking aid.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Breg Inc.
FDA (openFDA device enforcement)
Free recall alerts
Get alerted about new Connecticut recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.
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.