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 30, 2022
Outset Tablo Console Model Number: PN-0003000 Model Number: PN-0006000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Outset Medical, Inc.
FDA (openFDA device enforcement)
Reported Mar 25, 2022
FSIS Issues Public Health Alert for Ready-to-Eat Chicken Meal Kits Due to Misbranding and Undeclared Allergens
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Taylor Farms New England Inc.
USDA FSIS
Reported Mar 23, 2022
Safe-T PLUS Pediatric/Infant Lumbar Puncture Tray, 22 g x 1.5" Spinal Needle with Manometer
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bard Peripheral Vascular Inc.
10 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 23, 2022
BioPlex 2200 REF 12000650 SYPH T PACK Syphilis Total & RPR Reagent Pack
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bio-Rad Laboratories, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 23, 2022
Taiyaki Variety Pack; 21.6 oz. (600g) 30 fish waffles in a units, 27 master cased to a pallet, 40 pallets to container.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fdmr, Inc. dba Suji's Korean Cuisine
FDA (openFDA food enforcement)
Reported Mar 23, 2022
Panther Fusion Extraction Reagent-X, REF PRD-04477, For use with Panther Fusion System, IVD, Rx only, Contents: FCR-X…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hologic, Inc.
FDA (openFDA device enforcement)
Reported Mar 23, 2022
Mycoplasma genitalium Control Panel (Inactivated Pellet)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Microbiologics Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 23, 2022
Honey BBQ Snack, NO MSG Seasoning packaged in the following sizes: 1. 685-A, Net Wt 21 lbs. (9.52kg). Part #020001456.…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.PS Seasoning & Spices, Inc.
4 more products in this recall
FDA (openFDA food enforcement)
Reported Mar 23, 2022
All Ice Cream and Ice Cream products within expiry; manufactured by Royal Ice Cream Company; manufactured in…
High riskUsing this product could cause serious injury, illness or death — stop using it now.The Royal Ice Cream Company Inc.
FDA (openFDA food enforcement)
Reported Mar 16, 2022
CIRRUS HD-OCT, Models 5000 AngioPlex and 6000 AngioPlex
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carl Zeiss Meditec, Inc.
FDA (openFDA device enforcement)
Reported Mar 16, 2022
Celltrion DiaTrust COVID-19 Ag Rapid Test, Reference No. CT-P60 D-2 02
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Celltrion USA Inc.
FDA (openFDA device enforcement)
Reported Mar 16, 2022
Del Monte Bubble Fruit - Tropical Mixed Fruit Cup Snacks. Mixed fruit and popping boba with sweetened juice. 3.5 0z (4…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Del Monte Foods Inc.
FDA (openFDA food enforcement)
Reported Mar 16, 2022
Factor 75 - Fiery Beef & Black Bean Chili 12.7oz plastic tray sold as single serve meal to end consumer
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Factor
FDA (openFDA food enforcement)
Reported Mar 9, 2022
Alinity m Integrated Reaction Units (IRU)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Molecular, Inc.
FDA (openFDA device enforcement)
Reported Mar 9, 2022
Acorn 130 Stairlift, Brooks 130 Stairlift, Acorn 180 Stairlift, and Acorn Outdoor Stairlift
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Acorn Stairlifts, Inc.
FDA (openFDA device enforcement)
Reported Mar 9, 2022
AU/DxC AU Magnesium, Catalog/REF Number OSR6189, UDI 15099590010850
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported Mar 9, 2022
Titanium MPJ (Toe Implant) TOE JOINT TITANIUM NPC SM, Part ID 16813
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioPro, Inc.
9 more products in this recall
FDA (openFDA device enforcement)
Reported Mar 9, 2022
da Vinci Xi and X 12-8 mm Conductive Cannula Reducer, REF: 470381-11
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
FDA (openFDA device enforcement)
Reported Mar 9, 2022
Favorite Day Carrot cake soft bake cookies Net Wt 8 oz. (227g) UPC 0 885239 25803 3 packaged in gable top carton 6…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.J & M Foods, Inc.
FDA (openFDA food enforcement)
Reported Mar 2, 2022
Dole 10oz Very Veggie UPC: 0-71430-01008-2 SKU: 532
High riskUsing this product could cause serious injury, illness or death — stop using it now.Dole Fresh Vegetables Inc.
54 more products in this recall
FDA (openFDA food enforcement)
Reported Mar 2, 2022
Diastatic Malt Powder 50lb bag - up to 50 bags per pallet Malt Products Corporation
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Malt Products Corporation
FDA (openFDA food enforcement)
Reported Mar 2, 2022
Endurant, Endurant II and Endurant IIs Stent Graft System: Medtronic Endurant Stent Graft System Model/REF…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Vascular, Inc.
FDA (openFDA device enforcement)
Reported Mar 2, 2022
IPELA FHD PTZ TILE KITS with Axis cameras used in combination with Natus Neuroworks/Sleepworks software
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Natus Neurology dba Excel Tech., Ltd. (XLTEK)
FDA (openFDA device enforcement)
Reported Feb 23, 2022
bellavista 1000 ventilator, Catalog #301.100.030 and bellavista 1000e ventilator, 301.100.130. The bellavista…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Vyaire Medical
FDA (openFDA device enforcement)
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Other states
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.