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 Mar 20, 2024
CARTO VIZIGO Bi-Directional Guiding Sheath, REF D128502 The CARTO VIZIGOTM Bi-Directional Guiding Sheath is designed to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biosense Webster, Inc.
FDA (openFDA device enforcement)
Reported Mar 20, 2024
EasyPoint Needle, 25G x 5/8", REF: 82091
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Retractable Technologies, Inc.
FDA (openFDA device enforcement)
Reported Mar 13, 2024
MIC* Gastric-Jejunal Feeding Tube with ENFit Connectors: a) MIC* Gastric-Jejunal Feeding Tube Kit with ENFit Connector…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Avanos Medical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 13, 2024
MRI system: Vantage Orian, Vantage Fortian, Model: MRT-1550
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Canon Medical System, USA, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 13, 2024
BD Pyxis: MedStation ES, REF: 323; Anesthesia Station ES, REF: 327; MedStation ES Tower, REF: 352;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
FDA (openFDA device enforcement)
Reported Mar 13, 2024
Crumbled Cotija Net Wt. 5.6 lbs (300/0.3oz), Net Wt. 7.5 lbs (300/0.4 oz) Fontana, CA 92336 Plant #06-00333 Classic…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Castle Importing, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Mar 13, 2024
The Apollo Onyx Delivery Microcatheter (AOMC) is a DMSO-compatible, single-lumen, end hole catheter designed for the…
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 Mar 6, 2024
IdentiTi ALIF Standalone Interbody System: Part Number/Description 132-10-85-250 / IdentiTi ALIF SA Graft Bolt, 08.5 x…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alphatec Spine, Inc.
FDA (openFDA device enforcement)
Reported Mar 6, 2024
Medtronic Duet External Drainage and Monitoring System, Interlink Injection Sites, REF 46913, Sterile EO, Rx Only. Used…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Medtronic Neurosurgery
4 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 6, 2024
MUTTI Crushed Tomatoes; Polpa; Net Wt 27.9 OZ (1lb 11.9 OZ) 790g; UPC 85469300071
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mutti USA Inc.
FDA (openFDA food enforcement)
Reported Mar 6, 2024
Marketside Southwest Chopped Kit 10.3 oz. UPC 681131305129
High riskUsing this product could cause serious injury, illness or death — stop using it now.Ready Pac Foods Inc.
3 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 28, 2024
Meta Psyllium Fiber Capsules packaged as 100 count or 160 count PET bottles - 12 bottles per case.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Procter & Gamble Company
FDA (openFDA food enforcement)
Reported Feb 21, 2024
BIOFIRE Blood Culture Identification 2 (BCID2) Panel when used with: BD BACTEC Lytic Anaerobic medium BD BACTEC Peds…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 21, 2024
Microbiologics Enteric Pathogens Control Panel (Inactivated Pellet), REF 8184.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Microbiologics Inc.
FDA (openFDA device enforcement)
Reported Feb 21, 2024
Samsung Digital Diagnostic Mobile X-ray System, Model GM85.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.NeuroLogica Corporation
FDA (openFDA device enforcement)
Reported Feb 14, 2024
FilmArray Pneumonia Panel Plus (Pneumoplus), REF: RFIT-ASY-0143, CED 2797, IVD, Rx Only (30 test kit)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 14, 2024
Guardian 4 Glucose Sensor, REF: MMT-7040A, MMT-7040C1, MMT-7040C2, MMT-7040C3, MMT-7040D1, MMT-7040D2, MMT-7040MA,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic MiniMed, Inc.
FDA (openFDA device enforcement)
Reported Feb 14, 2024
Total immunoglobulin M (IgM total) IVD, kit, nephelometry/turbidimetry
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Feb 7, 2024
the original BENNY T'S VESTA DRY HOT SAUCE GHOST NET WT. 1.5OZ INGREDIENTS: Fresh Chilies, Onions, Breadcrumbs…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Benny Ts Vesta Inc. dba Vesta Firey Gourmet Toppings
4 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 7, 2024
NovoTHOR Whole Body Light Pod, Gen 3.0 (1) Product Code S2188 - Reg (2) Product Code S2189 - Reg PRX (3) Product Code…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.THOR Photomedicine Ltd.
FDA (openFDA device enforcement)
Reported Jan 31, 2024
Accure Laser System, Model: PFMS00004
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Accure Acne, Inc.
FDA (openFDA device enforcement)
Reported Jan 31, 2024
PANTHER FUSION System REF 9121010000 The Panther System is an integrated nucleic acid testing system which fully…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hologic, Inc.
FDA (openFDA device enforcement)
Reported Jan 31, 2024
R&B Chocolate Chips Croissant Twist
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lecoq Cuisine Corporation
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jan 31, 2024
Power Knee, REF: PKA10001, and PKA10003; with Power Knee Battery, REF: PKA10002
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ossur H / F
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.