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 48,122 notices were distributed nationwide, so they reach Connecticut too — those are in the archive.
Reported Jun 8, 2016
The ARCHITECT Estradiol Kit Intended to measure estradiol, an estrogenic steroid, in plasma.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Laboratories
FDA (openFDA device enforcement)
Reported Jun 8, 2016
Non-Vented Dispensing Pin with One-Way Valve and Luer Lock Ultrasite Valve Product Usage: Used for aspiration of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.B. Braun Medical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 8, 2016
Novocastr Liquid Mouse Monoclonal Antibody Renal Cell Carcinoma Marker (RCC) is recommended for use as part of a panel…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leica Microsystems, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 8, 2016
AllergiEnd ST-9 Multiple Skin Test Applicator (Item 1000) and AllergiEnd ST-9 Multiple Well Test Tray (Item (1001).…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medscience Inc.
FDA (openFDA device enforcement)
Reported Jun 8, 2016
Brilliance 64 Computed Tomography X-ray Systems Product Usage: Intended to produce cross-sectional images of the body…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 8, 2016
Dimension Vista 500 Intelligent Lab System running on software versions V.3.6.1 SP1 or V.3.6.2, Device listing #…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 8, 2016
¿Topicort (desoximetasone) Cream USP, 0.05%, Packaged in 5 g Tubes, Professional Sample Only, Rx Only. Mfd. by: Taro…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Taro Pharmaceuticals U.S.A., Inc.
FDA (openFDA drug enforcement)
Reported Jun 1, 2016
GE Healthcare, Discovery IGS 730. Indicated for use in generating fluoroscopic and rotational images of human anatomy.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Medical Systems, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 1, 2016
Mighty Leaf Tea Company Organic Ginger Peach Iced Tea; 100/1 oz. per case Item number 60001. UPC: 00656252600019
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mighty Leaf Tea
FDA (openFDA food enforcement)
Reported Jun 1, 2016
RayStation Therapy Treatment Planning System Stand-alone Software 3.0, 3.5, 4.0, 4.5 and 4.7., designed for treatment…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Raysearch Laboratories Ab
FDA (openFDA device enforcement)
Reported Jun 1, 2016
3.2 mm Three-fluted drill bit, sterile, Catalog ID # 03.010.060S Product Usage: Usage: The 3.2 mm Three-fluted Drill…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes (USA) Products LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 1, 2016
Zinc Oxide Powder (API) used in the manufacturing of dietary supplements .
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Zochem Inc.
FDA (openFDA food enforcement)
Reported May 25, 2016
Bunge Soy Clear Fry Oil OU, 35 lb., Manufactured by: Bunge Oils, Inc. Kearny, NJ 07032, UPC 00078684692026
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bunge Oil North America Inc.
23 more products in this recall
FDA (openFDA food enforcement)
Reported May 25, 2016
Lumenis M22 System Model Number: GA-0005400 (M22 IPL + YAG Module) with Acne Filter (KT-1014971).
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lumenis Ltd.
FDA (openFDA device enforcement)
Reported May 25, 2016
Michel et Augustin brand Petites baguettes butter cookies Dark Chocolate with a pinch of salt, NET WT. 1.58 oz (45g),…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Michel et Augustin Inc.
FDA (openFDA food enforcement)
Reported May 25, 2016
Colby Jack cheese, 8 oz. and 16 oz, Vacuumed plastic pouches
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Msu Dept Of Fd Sci Dairy Plant
FDA (openFDA food enforcement)
Reported May 25, 2016
Royal Snacks Jalapeno Pistachio Royal Size
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Royal Snacks Inc.
FDA (openFDA food enforcement)
Reported May 25, 2016
ADVIA Chemistry Triglyceride_2, concentrated; TRIG_c; Catalog # SMN # 10697575. For in vitro diagnostic use in the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported May 25, 2016
Sugarfina Chocolate Malt Balls UPC Code 840278113565 SKU K1159
High riskUsing this product could cause serious injury, illness or death — stop using it now.Sugarfina, LLC
FDA (openFDA food enforcement)
Reported May 25, 2016
COMMERCIAL WHEAT GERM 274000, 50.00 lbs. (22.68 kg); UPC Code: 0-26938-46535-3
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Unfi
FDA (openFDA food enforcement)
Reported May 18, 2016
Direct Drive Clip Applier CA090, indicated for ligation of tubular structures or vessels in laparoscopic and general…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Applied Medical Resources Corp.
FDA (openFDA device enforcement)
Reported May 18, 2016
Ascom Mobile Monitoring Gateway (versions 4.1.1 and 4.2.0) and Ascom Unite Connect for Nurse Call (version 2.2.0).
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ascom US, Inc.
FDA (openFDA device enforcement)
Reported May 18, 2016
Arctic Sun Temperature Management System, 5000, 100-120V and 220-240V The product is a thermal regulating system…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard, Inc.
FDA (openFDA device enforcement)
Reported May 18, 2016
Reporte De Notificacion De Retirada 041-2016 (Masa Hervida Rellena de Cerdo)
High riskUsing this product could cause serious injury, illness or death — stop using it now.Recalling firm not stated
USDA FSIS
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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.