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.
3,080 stored notices name Connecticut, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,765 notices were distributed nationwide, so they reach Connecticut too — those are in the archive.
Reported Mar 15, 2023
Given Imaging SmartBar Cereal Bar; Net Weight 2.53 oz (72 g); Ingredients: glucose syrup, soy crisps, oats, pea…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Given Imaging Ltd.
FDA (openFDA food enforcement)
Reported Mar 15, 2023
PREAT NOBIL GRIP, product numbers 0102000 and 01202000-3 (3 pack), 5-ml vials packaged in pouches, dental anaerobic…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Preat Corp.
FDA (openFDA device enforcement)
Reported Mar 8, 2023
Alaris PC Unit 8015 utilizing 802.11 b/g or 802.11 a/b/g wireless network cards, with IP addresses from x.x.x.224 to…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
FDA (openFDA device enforcement)
Reported Mar 8, 2023
Drizzilicious Mini Rice Cake bites Net Wt. 4oz and .74oz Bags Birthday Cake UPC: 857900005402 and 857900005419 Packaged…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Snack Innovations Inc.
7 more products in this recall
FDA (openFDA food enforcement)
Reported Mar 1, 2023
Rao's Made for Home Slow Simmered Soup, labeled as Chicken & Gnocchi, Soup in 16-ounce glass jars, 6 jars per case.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Sovos Brands Intermediate, Inc.
FDA (openFDA food enforcement)
Reported Feb 22, 2023
HydroMID 4Fr Single Lumen - Basic Kit, Model Number 80004002
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Access Vascular, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Feb 15, 2023
The Covera Vascular Covered Stent is a flexible, self-expanding endoprothesis comprised of ePTFE encapsulating a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
FDA (openFDA device enforcement)
Reported Feb 8, 2023
DR SNACK brand Crystal Ginger; Net Wt. 7.00 oz (0.20kg); Net 6oz; and Net 10 oz.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.B.C.S. International Corporation
FDA (openFDA food enforcement)
Reported Feb 8, 2023
Catalog Number / Product Description 0601600 2.7F Broviac CV Catheter Repair Kit 0601610 4.2 Fr Broviac CV Catheter…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
FDA (openFDA device enforcement)
Reported Feb 8, 2023
James Farm brand Frozen Red Raspberries; 2-5lb Bags; NET WT 10 LB (4.5 kg); KEEP FROZEN; IQF; Individually Quick…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Exportadora Copramar Ltda.
FDA (openFDA food enforcement)
Reported Feb 8, 2023
GORE CARDIOFORM Septal Occluder, REF: GSX0030A
Moderate riskThis product could cause temporary or reversible health problems — stop using it.W L Gore & Associates, Inc.
FDA (openFDA device enforcement)
Reported Feb 1, 2023
Avery's Savory Popcorn Gourmet Popcorn All Flavors packaged in clear plastic flexible bags heat sealed, unit size 1.5…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Averys Savory Popcorn, LLC
FDA (openFDA food enforcement)
Reported Feb 1, 2023
Slick Set Cuffed Endotracheal Tube and Stylet Set, oral/nasal. Intended for patients requiring endotracheal intubation
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 18, 2023
BD Pyxis MedBank System - Product Label/labeling pending
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
FDA (openFDA device enforcement)
Reported Jan 18, 2023
Dole Chopped Kit BBQ Ranch Green Cabbage, Green Leaf Lettuce, Kale, Carrots, Red Cabbage, Green Onions, Fried Onions,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Dole Fresh Vegetables Inc.
16 more products in this recall
FDA (openFDA food enforcement)
Reported Jan 18, 2023
Codman Surgical Patties, Part number 801400; SURG PATXRAY 1/2X1/2-200; Lot 6396457
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp.
FDA (openFDA device enforcement)
Reported Jan 18, 2023
RadiaLux Lighted Retractor (Pink), REF: 50-101-1
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.
FDA (openFDA device enforcement)
Reported Jan 18, 2023
Beijing Hawthorne Candy
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Northern Food I/E Inc.
FDA (openFDA food enforcement)
Reported Jan 18, 2023
VENTANA PD-L1 (SP142) VENTANA PD-L1 (SP142) Assay (Class III, US IVD) 07709374001 VENTANA PD-L1 (SP142) Assay (CE IVD…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ventana Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Jan 11, 2023
Various Custom Surgical Instrument Disposable Kits: Part Numbers / Product Description 26000004M Custom Lasik Kit…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Windstone Medical Packaging, Inc.
FDA (openFDA device enforcement)
Reported Jan 4, 2023
Part Number/Part Description: 30-0033-S 30mm Acutrak¿ Fusion Device 6mm Nose AM-0025-S 25.0mm Acutrak¿ 4/5 Bone Screw…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Acumed LLC
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jan 4, 2023
"Lukai sweetened jujube"; 8.3 ounces; red and yellow packaging; back panel states: "Name: Ejiao dates; Ingredients: a…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Northern Food I/E Inc.
FDA (openFDA food enforcement)
Reported Dec 28, 2022
InPen Diabetes Management App, part of the InPen System, REF: MMT-105ELBLNA, MMT-105ELGYNA, MMT-105ELPKNA,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Companion Medical, Inc.
FDA (openFDA device enforcement)
Reported Dec 28, 2022
The Natus Cranial Access Kit is designed to be a complete, single use and disposable accessory and instrumentation set…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natus Medical Incorporated
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.