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 48,122 notices were distributed nationwide, so they reach Connecticut too — those are in the archive.
Reported Oct 23, 2013
Talenti German Chocolate Cake Gelato, One Pint (473 mL), Crafted By: Talenti, Marietta, GA 30062.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Talenti Gelato
FDA (openFDA food enforcement)
Reported Oct 9, 2013
Lactate Membrane units for E7077 Electrode Radiometer Medical ApS. The intended use is in vitro testing of samples of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Radiometer America Inc.
FDA (openFDA device enforcement)
Reported Oct 2, 2013
Blythedale Farm Vermont Brie, 7 oz. wrapped disc in plastic cup UPC Code: 762713669010
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Blythedale Farm Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Oct 2, 2013
Monaco RTP System Radiation treatment planning
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 2, 2013
Invacare Power Wheelchair, one per box To provide mobility to a person restricted to a sitting position.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Invacare Corporation
FDA (openFDA device enforcement)
Reported Oct 2, 2013
DRI Cocaine Metabolite Assay, labeled as Multigent Cocaine Assay for Abbott Laboratories. 100 ml, IVD Mfg by:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Microgenics Corp.
FDA (openFDA device enforcement)
Reported Oct 2, 2013
JAMES FARM brand CUT GREEN BEANS (EJOTES CORTADOS), FRESH FROZEN, NET WT. 32 OZ. (2 LBS.) 907 g, UPC 7 60695 01004 2,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Restaurant Depot
FDA (openFDA food enforcement)
Reported Oct 2, 2013
Stryker Vision Mounting Arm, for use with other Stryker Endoscopy medical device products for human patients. Model…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Endoscopy
FDA (openFDA device enforcement)
Reported Oct 2, 2013
Terumo Pall AL6X Arterial Blood Line Filter, labeled in part Terumo Cardiovascular Systems Corporation, packaged as…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
FDA (openFDA device enforcement)
Reported Sep 25, 2013
3M Scotchcast, Wet or Dry Cast Padding, Catalog Numbers WDP2, WDP3, WDP4, and WDP6. Intended for use in constructing…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.3M Company - Health Care Business
FDA (openFDA device enforcement)
Reported Sep 25, 2013
Liquid Yeast Cream, Bulk, in tanker truck quantities, refrigerated 33F-45F
Moderate riskThis product could cause temporary or reversible health problems — stop using it.American Yeast Corporation
FDA (openFDA food enforcement)
Reported Sep 25, 2013
Osseotite 2 Certain Prevail 5mm(D)X 4.1mm (P) X X 11.5mm (L) Dental Implant Product Usage: Surgical placement in the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet 3i, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 25, 2013
Olde Cape Cod Chipotle Ranch dressing, 16 oz. Item Number: 90997-11630
High riskUsing this product could cause serious injury, illness or death — stop using it now.Cains Foods LP
FDA (openFDA food enforcement)
Reported Sep 25, 2013
GE Healthcare, CARESCAPE Monitor B850. Intended for use in multiple areas within a professional healthcare facility.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
4 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 25, 2013
Pills bury Cinnamon Rolls with Icing, CINNA BON, USPC 1800000501, 1800052230, 12.4 oz and 2-pack USPC 1800045675,2-…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.General Mills, Inc.
FDA (openFDA food enforcement)
Reported Sep 25, 2013
ACL TOP (Base); PN 0000280000 Bench top, fully automated, random access analyzer designed specifically for in vitro…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Instrumentation Laboratory Co.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 25, 2013
Hydroxocobalamin MDV 5 mg/mL (5,000 mcg/mL) Inj., 10 mL vial X 3, Eastern States Compounding Pharmacy, Littleton, NH…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Northern New England Compounding Pharmacy LLC
FDA (openFDA drug enforcement)
Reported Sep 25, 2013
Responder 5 is a nurse call communication system that connects patients with staff in a hospital. The nurse call system…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Rauland-Borg Corp.
FDA (openFDA device enforcement)
Reported Sep 25, 2013
AEQUALIS Reversed II or AEQUALIS Reversed Fracture Impactor. These products are contained within the Aequalis reversed…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tornier, Inc.
FDA (openFDA device enforcement)
Reported Sep 25, 2013
Juno DRF System. Mobile X-ray system These are general, multi-function x-ray systems capable of routine radiographs and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Villa Radiology Systems LLC
FDA (openFDA device enforcement)
Reported Sep 18, 2013
BD Microtainer Quikheel Lancet 1.0 mm incision Depth 2.5 mm Incision Length REF 368101 Rx Only Becton, Dickinson and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Company
FDA (openFDA device enforcement)
Reported Sep 18, 2013
OPERON D850 Surgical Table Product Usage: Surgical Table
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Berchtold Corp.
FDA (openFDA device enforcement)
Reported Sep 18, 2013
*** 1) Cat. 4341B; Qty. 10; Thoracentesis Tray; With Catheter; Sterile; CareFusion; 1500 Waukegan Road; McGaw Park, IL…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carefusion 2200 Inc.
FDA (openFDA device enforcement)
Reported Sep 18, 2013
ADVIA Centaur Folate (100 Tests), SMN 10310308, Cat No. 06367974 In vitro diagnostic use in the quantitative…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
3 more products in this recall
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.