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 Aug 19, 2026Updated Aug 25, 2026
navify Digital Pathology (on-prem) v2.5, Material Number 10092343001 navify Digital Pathology (Cloud) v2.5. Material…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ventana Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Aug 12, 2026Updated Sep 16, 2026
Oribe Serene Scalp Densifying Shampoo, packaged in 8.5 fl. oz. (250 mL) bottles with UPC 840035231242 and 33.8 fl. oz.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.KAO USA Inc.
FDA (weekly enforcement report)
Reported Aug 12, 2026
Brand Name: Quantum Rehab Product Name: Quantum 4Front 2 Model/Catalog Number: Quantum 4Front 2 Software Version:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pride Mobility Products Corp.
12 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 5, 2026
L-Cath PICC S/L Peripherally Inserted Central Catheter: 26ga (1.9F) 0.60mm x 30cm, REF: 384539; 18ga (3.5F) 1.15mm x…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Argon Medical Devices, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 5, 2026
Permobil M3 Corpus Power Wheelchair with Heavy Duty Shock REF:120031, Model version 3
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Permobil Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 5, 2026
Resmed Astral 100/150 Resmed Astral 100/50 is a ventilator system that provides continuous or intermittent ventilatory…
High riskUsing this product could cause serious injury, illness or death — stop using it now.ResMed Ltd.
FDA (openFDA device enforcement)
Reported Aug 5, 2026
AMS ALIGNED MEDICAL SOLUTIONS medical convenience kits labeled as: 1) ENT Pack, Part Number AMS10411B; 2) ENT Pack,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Windstone Medical Packaging, Inc.
11 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 29, 2026
Fusia, Asian Inspirations, Kimchi & Tofu Kimbap, 8.1 OZ (230 g), Paper Film Wrapper, 12 packages per case , 6 ea:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Gellert Global Group
FDA (openFDA food enforcement)
Reported Jul 29, 2026
MiniMed Go App, Model: MMT-8600 (iOS), MMT-8601 (Android)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic MiniMed, Inc.
FDA (openFDA device enforcement)
Reported Jul 29, 2026
Pipeline Flex Embolization Device with Shield Technology, 3.00 mm x 12 mm 027 REF PED2-300-12. Intracranial aneurysm…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Micro Therapeutics, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 29, 2026
Penumbra System RED 68 Reperfusion Catheter REF: RED68KIT
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Penumbra, Inc.
FDA (openFDA device enforcement)
Reported Jul 29, 2026
SeaSpine Polyaxial Head REF Number: 41-3010
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Seaspine Orthopedics Corporation
FDA (openFDA device enforcement)
Reported Jul 22, 2026
Amy's ORGANIC SOUPS LENTIL LIGHT IN SODIUM NET WT. 14.5 OZ. (411 g) Microwave: Place soup in a microwave-safe bowl.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Amy's Kitchen Inc.
FDA (openFDA food enforcement)
Reported Jul 22, 2026
Ice Pop, D'Dioses Coconut, 4 oz (85 g), with UPC 710594511867
High riskUsing this product could cause serious injury, illness or death — stop using it now.D'Dioses Fruit Pops, Inc.
15 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 22, 2026
Ruby, Artichoke Hearts Quartered, 5 LB 8 OZ (2500 G) DRAINED WT 3 LBS 6 OZ (1550G), Can, 6 cans per case, Store in dry…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Gellert Global Group
FDA (openFDA food enforcement)
Reported Jul 22, 2026
da Vinci SP Instrument Arm Drape, SP, 1-PACK, Part Number: 430013-13, 430013-15
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
FDA (openFDA device enforcement)
Reported Jul 22, 2026
functional formularies LIQUID HOPE ORGANIC WHOLE FOODS MEAL REPLACEMENT PEPTIDE FORMULA BERRY MEDLEY NET WT. 12 OZ…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nutricia North America
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jul 22, 2026
Orthofix MINIRAIL, STANDARD LENGTHENER Model/Catalog Number: M101, Unilateral orthopedic/trauma external fixation device
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Orthofix U.S. LLC
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 15, 2026
Intracept Access Instruments, Description/REF: INTRACEPT ACCESS INSTRUMENTS- DRILL/RLV0035, INTRACEPT ACCESS…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Neuromodulation Corporation
FDA (openFDA device enforcement)
Reported Jul 15, 2026
Brand Name: Fletcher CT/MR Shielded Applicator Set Product Name: Intracavitary Remote Afterloading Applicator Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 15, 2026
5008X Blood Tubing Set, 24 units per case. Includes the below model numbers and descriptions. 1. 5008X HD Pre-Flush…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fresenius Medical Care Holdings, Inc.
FDA (openFDA device enforcement)
Reported Jul 8, 2026
OTP5000 THORA/PARA TRAY, 5FR, NON-VALVED UDI-DI Code: 0110885403284748 PIG1260T SAFE-T-CENTESIS TRAY 6FR X 16CM UDI-DI…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Access Systems, Inc.
13 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 8, 2026
Covidien Shiley Disposable Decannulation Plug REF DDCP UDI-DI code: 10884522004060 Product Codes that include the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien LLC
FDA (openFDA device enforcement)
Reported Jul 8, 2026
Breathing circuit set, coaxial: REF: 260127, 260128, 260167, 260168 used with HAMILTON-C1, HAMILTON-T1 and HAMILTON-MR1…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hamilton Medical AG
1 more product in this recall
FDA (openFDA device enforcement)
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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.