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 48,100 notices were distributed nationwide, so they reach Kentucky too — those are in the archive.
Reported Oct 5, 2022
BD Pyxis MedBank Cabinet Software v2.1.2.9 Legacy MedBank Cabinets with Matrix Drawers include: . CUBEX MedFlex…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
FDA (openFDA device enforcement)
Reported Oct 5, 2022
Ambra PACS, Ambra ProViewer. Software for use as a primary diagnostic and analysis tool for diagnostic images.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DICOM Grid, Inc. d/b/a Ambra Health
FDA (openFDA device enforcement)
Reported Oct 5, 2022
MEDLINE CLEARPRO DOUBLE SWIVEL CLOSED SUCTION CATHETER, flat peel pouch EA, 10 EA per Inner Carton (IC), 20 EA/2 Inner…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.MEDLINE INDUSTRIES, LP - Northfield
2 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 5, 2022
Mother's Touch Complete Nutrition for New Babies Net WT. 13.8 OZ (391.6g) packaged in a white plastic circular…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Mothers Touch Formula
FDA (openFDA food enforcement)
Reported Oct 5, 2022
t:slim X2 insulin pump; t:slim X2 insulin pump with Dexcom G5; t:slim X2 insulin pump with Basal-IQ technology; t: slim…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tandem Diabetes Care Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 28, 2022
BD MaxGuard Extension Set with 4-way stopcock, REF: M4058
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carefusion
8 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 28, 2022
Grappler Suture Anchor, Titanium, 3.0 x 10mm, Sterile Kit, REF: P44-110-3010-SK, for use within the Grappler Suture…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Paragon 28, Inc.
FDA (openFDA device enforcement)
Reported Sep 21, 2022
MicroClave Clear Neutral Connector. A bidirectional connector used as an accessory to an intravascular catheter placed…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 21, 2022
Verify SixCess Challenge Pack. Used to confirm that critical parameters of steam sterilization have been reached within…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Steris Corporation Hopkins Facility
FDA (openFDA device enforcement)
Reported Sep 14, 2022
Abbott Alinity m SARS-CoV-2 CTRL Kit, REF 09N78-085, each kit contains 12 x 1.3mL CTRL - and 12 x 1.3 mL CTRL +, For In…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Molecular, Inc.
FDA (openFDA device enforcement)
Reported Sep 14, 2022
Product Description/Item: ChemoLock Bag Spike, 10 units/CL-10-10; ChemoLock BAG SPIKE w/ ADDITIVE PORT, DRY…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 14, 2022
Philips BiPAP A30, Rx Only. To provide noninvasive ventilation support for patients with obstructive sleep apnea…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Philips Respironics, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 7, 2022
Pentacam AXL Wave REF 70020. Used to image the anterior segment of the eye.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Oculus Optikgeraete GmbH
2 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 7, 2022
Priyems Sambar Spicy Lentil Soup 800 grams (1.76 lbs) UPC 8 61754 00010 0, 8 retail units per wholesale case, Frozen
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Yem Foods LLC
3 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 31, 2022
NUCLISENS easyMAG Magnetic Silica, REF 280133, 24 x 1.2mL bottles/kit.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.bioMerieux, Inc.
FDA (openFDA device enforcement)
Reported Aug 31, 2022
Organic Amaranth Grain Gluten Free, Bob's Red Mill brand, packaged in Standup Pouch (24oz). Each case consists of 4/24…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bob's Red Mill Natural Foods, Inc.
FDA (openFDA food enforcement)
Reported Aug 31, 2022
Capriole Goat Cheese, Fresh Goat Cheese, Wasabi 5 pound and 8oz logs
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Capriole, Inc.
FDA (openFDA food enforcement)
Reported Aug 31, 2022
INTERA 3000 Hepatic Artery Infusion Pump, 30 mL, Sterile, Rx Only. implantable infusion pump.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Intera Oncology, Inc.
FDA (openFDA device enforcement)
Reported Aug 31, 2022
Vanta Clinician Programmer Application, Model A71200. For programming of the Medtronic Model 977006 Vanta implantable…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neuromodulation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 24, 2022
Kabobs The Hors d'oeuvre Specialist TOMATO, BASIL & MASCARPONE ARANCINI 180 COUNT Prepared by: Kabobs, Inc., 5423 North…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kabobs Acquisition Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Aug 24, 2022
ARIES SARS-CoV-2 Assay
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Luminex Corporation
FDA (openFDA device enforcement)
Reported Aug 24, 2022
Power electronic box, Part #AS-0066, subassembly for the MyoCycle MC-2.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Myolyn Inc.
FDA (openFDA device enforcement)
Reported Aug 17, 2022
The Cholestech LDX¿ System combines enzymatic methodology and solidphase technology to measure total cholesterol, HDL…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alere San Diego, Inc.
FDA (openFDA device enforcement)
Reported Aug 17, 2022
Clear American brand "Strawberry Punch Snow Cone" flavored sparkling water beverage with other natural flavors; 1-liter…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Refresco Beverages US Inc.
FDA (openFDA food 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.