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 May 17, 2017
Anthrex Bio-SwiveLock SP Vented, 5.5mm x 24.5 mm, Self-Punching
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arthrex, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported May 17, 2017
CooperSurgical lnflatoball Latex Rubber Pessary sold as an individual unit and also part of the lnflatoball Pessary…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CooperSurgical, Inc.
FDA (openFDA device enforcement)
Reported May 17, 2017
Mentor Smooth Round SPECTRUM Post- Operatively Adjustable Saline Breast Implant, Product Code: 350-1490, UDI/GTIN:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mentor Texas, LP.
FDA (openFDA device enforcement)
Reported May 17, 2017
Stryker PROFESS Registration Kit. The Stryker PROFESS Registration Kit is a member of the Navigation portfolio and is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
FDA (openFDA device enforcement)
Reported May 10, 2017
The JETSTREAM is a rotational atherectomy catheter system designed for use in debulking and treating vascular disease…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
FDA (openFDA device enforcement)
Reported May 10, 2017
Shandon Rapid Chrome Kwik-Diff Kit Part Number: 9990700 Shandon Rapid Chrome Kwik-Diff Reagent #3 Part Number 9990707…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Richard-Allan Scientific Company
FDA (openFDA device enforcement)
Reported May 10, 2017
Accu-Chek Connect Diabetes Management App versions 2.0.0, 2.0.1 and 2.1.0 for iOS and Android Product Usage: This is a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diabetes Care, Inc.
FDA (openFDA device enforcement)
Reported May 6, 2017
Perdue Foods LLC. Recalls Poultry Products Due to Possible Foreign Matter Contamination
High riskUsing this product could cause serious injury, illness or death — stop using it now.Gold Creek Foods, LLC
USDA FSIS
Reported May 3, 2017
Apple Cider with Potassium Sorbate, packed under the following labels: RUDY'S BLEND APPLE CIDER; 1 GAL. (3.78L), UPC: 8…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bevovations, LLC dba New England Apple Products Company
1 more product in this recall
FDA (openFDA food enforcement)
Reported May 3, 2017
HeartWare HVAD System Controller The HeartWare Ventricular Assist System (VAS is indicated for use as a…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Heartware
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 3, 2017
uNion Cervical Plate System Product Usage: The uNion Cervical Plate System is intended for anterior fixation of the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ulrich Medical USA Inc.
FDA (openFDA device enforcement)
Reported May 3, 2017
5.5mm Diameter x 500mm CoCr Straight Rod, Model number X077-0420. The product is packaged in plastic bags with one…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Xtant Medical Inc.
FDA (openFDA device enforcement)
Reported Apr 26, 2017
INFINITY Internal Hex Healing Abutment, 4.5mm Platform, 4.7mm CW-3mm CH Straight; Product Code: 20145473 Product Usage:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ace Surgical Supply Co., Inc.
FDA (openFDA device enforcement)
Reported Apr 26, 2017
AFC Edamame Soybeans in Pods, 8 oz , refrigerated, in cardboard container. UPC 0-23012-00261-9
High riskUsing this product could cause serious injury, illness or death — stop using it now.Advanced Fresh Concepts Corp.
FDA (openFDA food enforcement)
Reported Apr 26, 2017
Asher's Chocolate Co, Milk Chocolate (11481) Pretzel Cluster; Net Wt. 5 lb.; Asher's Chocolate Co, Milk Chocolate…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ashers Chocolates/Lewistown, Inc.
86 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 26, 2017
PGCL [poly (glycolide-co-caprolactone)] Absorbable Suture, Manufacturer CP Medical, Portland OR, Sterile, Product Codes…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CP Medical Inc.
FDA (openFDA device enforcement)
Reported Apr 26, 2017
Nutiva Nuture Vitality Organic Plant Protein Superfood 30 Shake - Vanilla; Product # PBP201 - 10-1.2 oz. packets;…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Nutiva
1 more product in this recall
FDA (openFDA food enforcement)
Reported Apr 26, 2017
Arrow EZ-IO Needle Set 45 mm 15 ga, Ref 9079.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Teleflex Medical
FDA (openFDA device enforcement)
Reported Apr 19, 2017
LIDIA'S MARINARA, NET WT 25 oz (708g), UPC 897712001018 --- Manufactured for Nonna Foods LLC Woodbury, NY 11797
High riskUsing this product could cause serious injury, illness or death — stop using it now.Nonna Foods
FDA (openFDA food enforcement)
Reported Apr 19, 2017
Specimen Gate Laboratory; Product Number: 5002-0180 Specimen Gate Laboratory is intended for use as a data processing…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.PerkinElmer Life and Analytical Sciences, Wallac, OY
FDA (openFDA device enforcement)
Reported Apr 19, 2017
Radiation Therapy Treatment Planning System, Model 4.5, 4.7, 5.0 RayStation is a software system designed for treatment…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Raysearch Laboratories Ab
FDA (openFDA device enforcement)
Reported Apr 19, 2017
CADD¿ Administration Set, 21-7339-24, Rx Only, Sterile EO.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD Inc.
FDA (openFDA device enforcement)
Reported Apr 19, 2017
Vulto Creamery Ouleout soft wash-rind raw milk cheese cut and wrapped in clear plastic
High riskUsing this product could cause serious injury, illness or death — stop using it now.Whole Foods Market
4 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 12, 2017
Dark Chocolate bars Choklad Mork Dark Chocolate, Net Wt. 3.5 OZ. AND Chokland Mork Dark Chocolate 70%, Net Wt. 3.5 OZ.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ikea North America Srvcs Inc.
5 more products in this recall
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.