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 Sep 27, 2017
K-Assay(R) Multi-Analyte Calibrator, REF KAI--016C, KAMIYA BIOMEDICAL COMPANY, Seattle, WA, IVD The K-ASSAY(R)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kamiya Biomedical Company, LLC
FDA (openFDA device enforcement)
Reported Sep 27, 2017
Spine Referencing Instrumentation, Spinous Process Clamp, Tall When used with a Medtronic StealthStation Navigation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 20, 2017
Spectra-System/Legacy Guided Surgery Handle Kit, Device Listing Number D245883. The Guided Handle Kit (G-HK) allows…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Implant Direct Sybron Manufacturing, LLC
FDA (openFDA device enforcement)
Reported Sep 20, 2017
Cell Marque, Podoplanin (D2-40 Mab), 7 mL, REF PA0796, IVD, The antibody is intended for in vitro diagnostic (IVD) use.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leica Biosystems Richmond Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 20, 2017
Makoplasty Partial Knee Application (PKA) Product Usage: The Robotic Arm Interactive Orthopedic System (RIO) is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mako Surgical Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 13, 2017
MOSAIQ Medical Charged-Particle Radiation Therapy System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Sep 13, 2017
Southeastern Mills, Biscuit Gravy Mix, Net Wt. 2.75oz (77g), 4.5oz (128g) flexible plastic packages.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Southeastern Mills Custom Seasoning Solutions
5 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 6, 2017
Papayas Maradol cavi, Grown and Packed by: CARICA DE CAMPECHE, DISTRIBUTED BY: AGROSONS LLC
High riskUsing this product could cause serious injury, illness or death — stop using it now.Agrosons LLC
FDA (openFDA food enforcement)
Reported Sep 6, 2017
Mary's Gone Crackers Original Crackers: Organic, Gluten Free, Non-GMO, Vegan. 6.5 oz. (184 g) box; Ingredients: Whole…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Mary's Gone Crackers, Inc.
FDA (openFDA food enforcement)
Reported Sep 6, 2017
iVue with Normative Database, Device Listing Number D185549. Product Usage: The iVue (K121739) is a non-contact, high…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Optovue, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 30, 2017
Demakes Enterprises, Inc. Recalls Chicken Sausage Product Due To Misbranding and Undeclared Allergens
High riskUsing this product could cause serious injury, illness or death — stop using it now.Demakes Enterprises, Inc.
USDA FSIS
Reported Aug 30, 2017
Fairway brand Cookies Blondie, 10 oz. Item Code 268492 XXXXXX or 263413 XXXXXX.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fairway Group Holdings Corp.
FDA (openFDA food enforcement)
Reported Aug 30, 2017
DBS Lead Depth Stop contained in Medtronic Deep Brain Stimulation (DBS) lead kits, models 3387/3387S, 3389/3389S, and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neuromodulation
FDA (openFDA device enforcement)
Reported Aug 30, 2017
Tissu-Trans Filtron 100, 3-TT-FILTRON 100. Product Usage: Intended for fat transfer and liposuction.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Shippert Medical Technologies
6 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 25, 2017
DiLuigi Foods Inc. Recalls Chicken Sausage Products Due to Misbranding and Undeclared Allergens
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DiLuigi Foods Inc.
USDA FSIS
Reported Aug 23, 2017
Arctic Sun 5000 Temperature Management System, 100-120 V North America and 100-120 V US
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard, Inc.
FDA (openFDA device enforcement)
Reported Aug 23, 2017
VNS Therapy¿ AspireHC¿ Generator, VNS Therapy¿ AspireSR¿ Generator. Model No. 105. Product Usage: United States…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cyberonics, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 23, 2017
Expresco Foods Inc. Recalls Chicken Skewer Products Due to Possible Listeria Contamination
High riskUsing this product could cause serious injury, illness or death — stop using it now.Expresco Foods Inc.
USDA FSIS
Reported Aug 23, 2017
Brivo MR355, Optima MR360 Product Usage: The Brivo MR355/Optima MR360 is a whole body magnetic resonance scanner…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Medical Systems, LLC
8 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 16, 2017
J.J. LAWSON BELGIUM CHOCOLATE ICE CREAM, 3 gallon round container
High riskUsing this product could cause serious injury, illness or death — stop using it now.Bliss Microcreamery, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Aug 16, 2017
iGUIDE Software 2.2 Product Usage: Control of accurate patient positioning with assistance of a 30 Tracking System in a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported Aug 16, 2017
Glipizide Extended-Release Tablets (anti-diabetic agent), 5 mg, packaged in 30-unit dose blister pack per carton, Rx…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Teva Pharmaceuticals USA
FDA (openFDA drug enforcement)
Reported Aug 15, 2017
Missa Bay, LLC Recalls Chicken Products Due To Misbranding and an Undeclared Allergen
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Missa Bay LLC
USDA FSIS
Reported Aug 9, 2017
Whole Foods Market Thai Shrimp Salad, Net Wt. 14 oz.. packaged in a clear clamshell container (refrigerated)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cafe Spice GCT dba Zaika Flavors
FDA (openFDA food 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.