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 Nov 21, 2012
Select Medical Products Vinyl Powder-Free Exam Gloves, Medium Model # 6370 and Large Model # 6371, 100 per box; 10…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Gulf South Medical Supply Inc.
FDA (openFDA device enforcement)
Reported Nov 21, 2012
Kentucky Rose, blue cheese Sizes could be 8oz packages, 1.5lbs packages, 3.5lbs packages, 7lbs packages, or 15lb wheel…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Kennys Farmhouse Cheese
3 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 14, 2012
Boule Con-Diff Hematology Control For in vitro diagnostic use as a control to monitor the performance of…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Clinical Diagnostic Solutions
4 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 14, 2012
Trochar Scalpel Instrument (Surgical Punch) OrthoPediatrics intramedullary rods (nails) are generally rod-shaped…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.OrthoPediatrics Corp.
FDA (openFDA device enforcement)
Reported Nov 14, 2012
AC Powered adjustable hospital bed, Prime Bed TL500, Distributed by: Primus Medical LLC, 8401 Southern Blvd, Boardman,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Primus Medical LLC
FDA (openFDA device enforcement)
Reported Nov 14, 2012
"***Sharpoint IQ Geometry Slit Knife Angled, Bevel Up***Surgical Specialties Corporation Reading, PA***REF 72-2740***"…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Surgical Specialties Puerto Rico Inc. dba Angiotech PR Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Nov 14, 2012
Peanut Butter Cup Ice Cream: 1) Velvet Supreme Peanut Butter Cup 1/2 gallon MFD BY VELVET ICE CREAM CO., INC UTICA,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Velvet Ice Cream Company
1 more product in this recall
FDA (openFDA food enforcement)
Reported Nov 7, 2012
HeartSine Samaritan(R) 300/300P PAD devices with serial numbers 0400000501 to 0700032917; 08A00035000 to 10A0070753;…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Heartsine Technologies, Limited
FDA (openFDA device enforcement)
Reported Nov 7, 2012
Myocardial Heart Wires Intended for temporary atrial and ventricular pacing and sensing during or after cardiac surgery…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Oscor, Inc.
FDA (openFDA device enforcement)
Reported Oct 31, 2012
DePuy Mitek VAPR Hook Electrode 3.5mm Hook Electrode with Integrated Handpiece Catalog Number: 227305 The DePuy Mitek…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Mitek, Inc., a Johnson & Johnson Co.
16 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 31, 2012
GE Seno Advantage 1.x, Seno Advantage 2.0, Seno Advantage 2.1 Seno Advantage 1.x, Seno Advantage 2.0, Seno Advantage…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
5 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 31, 2012
Kraft Jalapeno String Cheese, Net Wt 12 Oz (340 g); a natural low-moisture part-skim mozzarella cheese with jalapeno…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kraft Foods, Inc.
FDA (openFDA food enforcement)
Reported Oct 31, 2012
Perfusion System 8000, base 4 pump, 115V safety monitor included The Sarns Modular Perfusion System 8000 is indicated…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
5 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 24, 2012
Hemorrhoidal Circular Stapler and Accessories 33mm Product Usage: The PROXIMATE HCS Hemorrhoidal Circular Staplers,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Ethicon Endo-Surgery Inc.
FDA (openFDA device enforcement)
Reported Oct 24, 2012
GFS Individually Wrapped Blueberry Muffins, 1.8 Ounce, in 80 count case, Net Weight 9 lb./4.1 kg; Manufactured for…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ralcorp Frozen Bakery Products
FDA (openFDA food enforcement)
Reported Oct 17, 2012
3M Steri-Vac Gas Sterilizer/Aerator models 5XL and 8XL. 3M Steri-Vac Gas Sterilizer/Aerator is a compact unit designed…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.3M Company - Health Care Business
FDA (openFDA device enforcement)
Reported Oct 17, 2012
PREVI Isola System, Catalog numbers 29500 and 29500R, bioMerieux, Inc., Durham, NC. Intended to perform the inoculation…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomerieux Inc.
FDA (openFDA device enforcement)
Reported Oct 17, 2012
FRESH SELECTIONS by Kroger" Tender Spinach NET WT 10 OZ (283g) BEST IF USED BY 09/16/12 Product of USA 10:09…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Kroger Co.
FDA (openFDA food enforcement)
Reported Oct 17, 2012
diet Orange Crush, no calorie orange soda, 2 L (2.1 QT), UPC 078000013979
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pepsi Bottling Group Nashville
FDA (openFDA food enforcement)
Reported Oct 17, 2012
Battery, 100/115V (Includes charger and connecting cable) The Sarns" Centrifugal System is indicated for use in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
4 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 10, 2012
IR1200, IR1250(IR1200 Plus), 2020 and One Touch(R) Ping(R) Insulin Pump glucose management system. The device is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Animas Corporation
FDA (openFDA device enforcement)
Reported Oct 10, 2012
Optilock 2.7 mm Screw Inserter. Intended Use: The OptiLock Upper Extremity Plating System is intended for fixation of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomet, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 10, 2012
Cantaloupes are packed in 6ct, 9ct, 12ct, 15ct, 18ct, cardboard cartons with the DFI Brand. "826 California Westside"…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Dfi Marketing Inc.
FDA (openFDA food enforcement)
Reported Oct 10, 2012
Endoscopic retrieval device. The disposable Raptor grasping device in intended to retrieve foreign bodies or resected…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.US Endoscopy Group Inc.
FDA (openFDA device enforcement)
Free recall alerts
Get alerted about new Kentucky recalls
One email when a matching recall is published. No account, no cost, unsubscribe in one click.
We email you about recalls and nothing else. Every send has a one-click unsubscribe, and you can change your preferences any time without an account.
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.