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.
3,084 stored notices name Connecticut, reported between Jun 20, 2012 and Nov 18, 2026. A further 48,828 notices were distributed nationwide, so they reach Connecticut too — those are in the archive.
Reported Sep 23, 2015
KellBran" CANDIES, INC. creamy rich caramel popcorn Net Wt. 8 oz. (226.64 Grams) ALLERGY INFO: Manufactured in a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kellbran Candies and Snacks Inc.
FDA (openFDA food enforcement)
Reported Sep 23, 2015
The Leica ASP200S/ASP300S Tissue Processor. Pathology and Hematology Departments. The Leica ASP200S/ASP300S Tissue…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Leica Microsystems, Inc.
FDA (openFDA device enforcement)
Reported Sep 23, 2015
Pointe Scientific autoHDL Reagent H7545 H7545-R1 in a bulk cube container or HDPE plastic bottle H7545-1000 kit…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Pointe Scientific, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 16, 2015
Black Currant Huckleberry, Brioche and Jam Ice Cream Bucket, 313, Jeni's Splendid Ice Creams, LLC, 3 gallons, plastic…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Jeni's Splendid Ice Creams LLC
133 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 16, 2015
Mindray DPM 7 Monitor, Multi Parameter Patient Monitor (with Arrhythmia Detection and Alarms) Intended to be used for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mindray DS USA, Inc. dba Mindray North America
FDA (openFDA device enforcement)
Reported Sep 16, 2015
ADVIA Centaur¿ Folate Ascorbic Acid/Ascorbic Acid Diluent; SMN 10316877. Used to prepare the Red Blood Cell hemolysate…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Sep 16, 2015
CDI 500 Blood Parameter Monitoring System. Provides continuous, on-line monitoring of the extracorporeal partial…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
FDA (openFDA device enforcement)
Reported Sep 9, 2015
FIRMap 60mm Catheter; Size: 60 mm; Length 50.4 inches French Size Diameter: 8.5F (2.84mm) Model number : USAR064060…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Abbott Electrophysiology
FDA (openFDA device enforcement)
Reported Sep 9, 2015
MicroVue Bb Plus EIA is packaged as a kit which contains all reagent components to perform the test. In vitro…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Diagnostic Hybrids Inc.
FDA (openFDA device enforcement)
Reported Sep 9, 2015
Neptune 2 Waste Management System Docking Station (120V and 230V), New and Refurbished Product Usage: The Stryker…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
FDA (openFDA device enforcement)
Reported Sep 2, 2015
ExacTrac 6.0.x Patient Positioning System, Radiation therapy. Intended to be used to place patients at an accurately…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Brainlab AG
FDA (openFDA device enforcement)
Reported Sep 2, 2015
Dimension Vista B¿2-Microglobulin Flex Reagent Cartridge (B2MIC); Product Usage: The B2MIC method is an in vitro…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Aug 26, 2015
American Science & Engineering Inc,Gemini Cabinet X-ray system.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.American Science & Engineering, Inc.
FDA (openFDA device enforcement)
Reported Aug 26, 2015
Magic3 Hydrophilic-coated Female Intermittent Urinary Catheters (6"), 10 Fr, (30/box), Product Code 51610. Intermittent…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.C.R. Bard, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 26, 2015
Friendly's Vienna Mocha Chunk Ice Cream Tub, 48 U.S. FL. OZ. UPC: 0-29839 00557-4
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Friendly Ice Cream Corp.
FDA (openFDA food enforcement)
Reported Aug 26, 2015
Getinge 86 Series Washer/Disinfector with G1 control system software, Model 8666 and Model 8668. For use in healthcare…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Getinge Disinfection Ab
FDA (openFDA device enforcement)
Reported Aug 26, 2015
Siemens Symbia S Series system, a diagnostic analog or digital detector based planar (2- dimensional) nuclear medicine…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 26, 2015
Bronchial Double Lumen Tube Set (Left), Sterile
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex, Inc.
8 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 26, 2015
2.0/2.4 Cannulated Screw Countersink Part # 210-24-002 NON-STERILE and 3.0/4.0 Cannulated Screw Countersink Part #…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Trilliant Surgical Ltd.
FDA (openFDA device enforcement)
Reported Aug 19, 2015
Oasis Coil Extension Cable used with Hitachi Oasis MRI System Product Usage: The Oasis MR system is an imaging device…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hitachi Medical Systems America Inc.
FDA (openFDA device enforcement)
Reported Aug 19, 2015
Invacare¿ Pronto¿ Air Personal Transporter (power wheelchair), Invacare Corporation, One Invacare Way, Elyria, Ohio,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invacare Corporation
FDA (openFDA device enforcement)
Reported Aug 19, 2015
Acadia Natural Spring Water, 16.9 Fl Oz, Distributed by FoodHold USA, Inc, Landover, MD 20785; Acadia Natural Spring…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Niagara Bottling, LLC
FDA (openFDA food enforcement)
Reported Aug 19, 2015
JAMES FARM GARDEN PEAS CHICHAROS, NET Wt. 40 OZ (2.5 LBS), FRESH FROZEN, UPC 7 60695 01000, product is packed in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Restaurant Depot
FDA (openFDA food enforcement)
Reported Aug 12, 2015
A Taste of the East maya brand Cashew Split, packaged and sold in various sizes: (a) Net Wt. 7oz. (198g) UPC 0 20843…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Maya Overseas Foods,Inc.
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.