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 8, 2017
Abdominoplasty Pack, Part numbers AMS3326(B, AMS4381, and AMS4381(B.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Windstone Medical Packaging, Inc.
123 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 1, 2017
AMT Bridle - Nasal Tube Retaining System Used with Nasogastric/Nasointestinal (NG/NI) tubes.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Applied Medical Technology Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 1, 2017
ETEST XM256 (Cefuroxime), Foam: 506958-506918; SPB: 412304-412305 ETEST is a quantitative technique for determining the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioMerieux SA
FDA (openFDA device enforcement)
Reported Mar 1, 2017
Tosoh Bioscience HLC-723G8 Analyzer for HbA1c testing.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tosoh Bioscience, Inc.
FDA (openFDA device enforcement)
Reported Mar 1, 2017
Keyspan High-High Speed USB to Serial Adapter Product Usage: The Reporting Software is an application which serves as…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tosoh Smd Inc.
FDA (openFDA device enforcement)
Reported Feb 22, 2017
Burts British Hand Cooked Potato Chips Sea Salt & Malted Vinegar 150gx10 and 40gx20
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bwi Inc.
FDA (openFDA food enforcement)
Reported Feb 22, 2017
Stryker Restoris RIO Reamer Handle, Offset, Mako Rx only Product Usage: The handle is used to hold surgical components…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mako Surgical Corporation
FDA (openFDA device enforcement)
Reported Feb 22, 2017
LIFEPAK 15 Monitor, Automated External Defibrillator (AED), Manual mode monitoring and therapy functions are intended…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Physio-Control, Inc.
FDA (openFDA device enforcement)
Reported Feb 22, 2017
CentraLink¿ Data Management System Software Versions: v13x,v14x,v15x The CentraLink system software is a network…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 15, 2017
Boston Scientific, EMBLEM S-ICD Programmer Model 3200 Programmer.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
FDA (openFDA device enforcement)
Reported Feb 15, 2017
Bariatric Bed - BAR600IVC
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invacare Corporation
3 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 15, 2017
Merge Eye Station. f/k/a: DFC-1024 & DFC-512 Digital Imaging System, WinStation, and WinStation Retinal Imager…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merge Healthcare, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 15, 2017
Sheridan/CF, Cuffed Tracheal Tube, Catalog # 5-10114 and Sheridan/HVT Cuffed Tracheal Tube, Catalog # 5-10315 A…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical
FDA (openFDA device enforcement)
Reported Feb 15, 2017
DANONE¿ DAIRY DRINK NUT AND CEREAL 7.7 FL OZ (229mL) bottles, UPC 36632 01421
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Dannon Company, Inc.
FDA (openFDA food enforcement)
Reported Feb 15, 2017
Potassium Chloride Oral Solution, USP, 10%, 20 mEq per 15 mL, packaged in 15 mL unit dose cups (NDC 66689-047-01), 50…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.VistaPharm, Inc.
FDA (openFDA drug enforcement)
Reported Feb 8, 2017
Jon Donaire Ice Cream Layer Cake, Deliciously moist white cake with rich, creamy strawberries & cream ice cream, NET WT…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Rich Products Corp.
3 more products in this recall
FDA (openFDA food enforcement)
Reported Feb 8, 2017
Whole Foods Markets Lobster Bisque Distributed by: Whole Foods Market, Englewood Cliffs, NJ 07652 UPC: 8-80632-00100
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Whole Foods Market Northeast Regional Office
FDA (openFDA food enforcement)
Reported Feb 1, 2017
Tryptic Soy Agar, Acumedia PN 7100 500g, 2Kg, 10Kg, and 50Kg sizes
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Acumedia Manufacturers, Inc.
FDA (openFDA device enforcement)
Reported Feb 1, 2017
Hitachi Oasis MRI System - C-Spine Coil
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hitachi Medical Systems America Inc.
FDA (openFDA device enforcement)
Reported Feb 1, 2017
SCC Soft Computer Softbank II software Product Usage: Supports single and multi-site transfusion services in healthcare…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Soft Computer Consultants, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Feb 1, 2017
Gonsalves Sugar Coated Almonds, Net Wt. 12 oz. Distributed by The Gonsalves Company, Smithfield, RI 02917 UPC number…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Henry Gonsalves Co.
FDA (openFDA food enforcement)
Reported Feb 1, 2017
Juno DRF; Model: 709020 Multi-function x-ray systems capable of routine radiograph and general fluoroscopy procedures.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Villa Radiology Systems LLC
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 25, 2017
Ambra PACS UDI: +AMBRHEALTHSOLUTIONS0/$$+7_V3.16.13.0R Software Version Number: V3.16.13.0 Intended for use as a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dicom Grid Inc.
FDA (openFDA device enforcement)
Reported Jan 25, 2017
PREMIER EHEC and PREMIER EHEC Bulk.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Meridian Bioscience Inc.
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.