Recalls distributed in Kentucky
These notices name Kentucky 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.
3,340 stored notices name Kentucky, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,122 notices were distributed nationwide, so they reach Kentucky too — those are in the archive.
Reported Aug 5, 2015
Fat Free Pasteurized Prepared Cheese Product: SOUTHHOME 12/12OZ AMERICAN FAT FREE YELLOW, 0788001319. ROUNDYS 12/12OZ…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dairy Farmers OF America Inc.
33 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 5, 2015
Paragon Laboratory Management
Moderate riskThis product could cause temporary or reversible health problems — stop using it.McKesson Technologies, Inc.
FDA (openFDA device enforcement)
Reported Aug 5, 2015
SYMMETRY SURGICAL DISPOSABLE TOWEL CLAMP, REF 19-4137, STERILE EO, Rx only. Apply clamps parallel to the skin with the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Symmetry Surgical, Inc.
FDA (openFDA device enforcement)
Reported Aug 5, 2015
Synthes TI Matrix Pre-Bent Maxillary Plate / 2mm ADVMNT/0.8mm THK/L and Synthes TI Matrix Pre-Bent Maxillary Plate /…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes (USA) Products LLC
FDA (openFDA device enforcement)
Reported Aug 5, 2015
ANSPACH - Fluted Drum, Side Cut only 10MM x 14MM , REF L-10DRC-G1 Cutting shaping bone including spine and cranium.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Anspach Effort, Inc.
33 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 29, 2015
Bausch & Lomb SofPort Advanced Optics Aspheric Lens
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bausch & Lomb Surgical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 29, 2015
Ring Transjugular Intrahepatic Access Set Product Usage: The Ring Transjugular Intrahepatic Access Sets are intended…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cook Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 29, 2015
Milex Vaginal-Hymenal Silicone Dilators Set of 4 P/N MX20 Product Usage: The CooperSurgical Milex Vaginal-Hymenal…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CooperSurgical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 29, 2015
ATTUNE FB PS ARTICULATION SURFACE SIZES 3-8 INTENDED USE: The Tibial Articulation Surface Trial snaps together with the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Orthopaedics, Inc.
9 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 29, 2015
ADVIA Centaur Tni-Ultra Assay; SMN 10317708 - 100 tests and SMN 10317709 -500 tests Product Usage: For in vitro…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Healthcare Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Jul 29, 2015
0702-001-350Q, Diverter Valve Assembly 0702-001-000, Neptune 2 Rover Ultra (120V) 0702-001-000R, Repair Neptune 2 Rover…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 29, 2015
Various OxyTOTE Portable Oxygen System regulators, Valve Integrated Pressure Regulator, one unit per package. Product…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Western / Scott Fetzer Company
FDA (openFDA device enforcement)
Reported Jul 22, 2015
Alere i flu, Alere i, Alere Influenza A & B; Part Number (PN) 425-024 The Alere" i Influenza A & B assay, performed on…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alere Scarborough, Inc. dba Binax, Inc.
FDA (openFDA device enforcement)
Reported Jul 22, 2015
Diet Bubba Cola, 20 FL. OZ (1.25 PT) 591 mL INGREDIENTS: CARBONATED WATER, HIGH FRUCTOSE CORN SYRUP, CARAMEL COLOR,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Dr. Pepper Snapple Group Inc.
FDA (openFDA food enforcement)
Reported Jul 22, 2015
Tortilleria Provincia Refrigerate After Purchase White Corn Tortillas, Net Wt. 16 oz, 0 89780 10000 1 & 64 oz, 0 89780…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tortilleria Provincia
2 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 15, 2015
Philips GoSafe Communicator 7000L Personal emergency response system.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lifeline Systems, Incorporated
FDA (openFDA device enforcement)
Reported Jul 15, 2015
Breast Pack - contains Devon Light Glove Used during surgery
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stradis Healthcare, LLC.
50 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 8, 2015
Axis-Shield Liquid Stable (LS) 2-Part HOMOCYSTEINE REAGENT; 100 test format, 1000 test format, and 200 test format; and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Axis-Shield Diagnostics, Ltd.
FDA (openFDA device enforcement)
Reported Jul 8, 2015
Etest Cefotaxime CT 256 WW and Etest Cefotaxime CT 256 US. in vitro diagnostic.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioMerieux SA
FDA (openFDA device enforcement)
Reported Jul 8, 2015
HeartWare Ventricular Assist System (HVAD) For use as a bridge-to-cardiac transplantation in patient who are at risk of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.HeartWare Inc.
FDA (openFDA device enforcement)
Reported Jul 8, 2015
Infinite F500, in vitro diagnostic. Product Usage: The Tecan Infinite F500 is a multifunctional microplate reader with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tecan US, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 1, 2015
Raw Macadamia Nuts, packaged in 8 oz. plastic cup, packaged under the Aurora and private labels as follows:Belmont…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Aurora Products, Inc.
FDA (openFDA food enforcement)
Reported Jul 1, 2015
BLUE BELL COUNTRY COOKIE VANILLA ICE CREAM & CHOCOLATE CHIP COOKIE SANDWICH 5.75 FL OZ (170 mL)
High riskUsing this product could cause serious injury, illness or death — stop using it now.Blue Bell Creameries, LP
285 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 1, 2015
LapSac Surgical Tissue Pouch. The current intended use for the LapSac Surgical Tissue Pouch is for isolating tissue…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cook 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.