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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.

3,388 stored notices name Kentucky, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,743 notices were distributed nationwide, so they reach Kentucky too — those are in the archive.

Food

Reported Oct 14, 2026Updated Oct 20, 2026

28 oz. Gatorade Lemon Lime, Gatorade Lemon Lime Zero, Gatorade Orange, and Gatorade Orange Zero.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Pepsico Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Oct 14, 2026Updated Oct 20, 2026

Spectral CT and Spectral CT 7500 RT; Software Version Numbers: 5.2.X (U.S.); 5.0.X, 5.2.X, 5.4.X (Outside U.S.); Model…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips Medical Systems

FDA (openFDA device enforcement)

Medical devices

Reported Oct 14, 2026Updated Oct 20, 2026

SEDIPLAST; Model/Catalog Numbers: S-100 and S-1000;

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Polymedco, Inc. / Polymedco Cancer Diagnostic Products, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Oct 14, 2026Updated Oct 20, 2026

Battle Bandage, REF: 32-700; Patrol IFAK Bag, Black - Advanced, REF: 81-125-BL; Patrol IFAK Bag, Multicam - Advanced,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Safeguard US Operating LLC

FDA (openFDA device enforcement)

Food

Reported Oct 14, 2026Updated Oct 20, 2026

Saint Francis Apizza Frozen Pepperoni Pizza, Net Weight: 17 oz. (482g), packaged individually in vacuum-sealed plastic,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Saint Francis Apizza LLC

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Oct 7, 2026Updated Oct 13, 2026

McKesson CONSULT hCG Urine Cassette, Model/ Part: FHC-A102/5001; Alere hCG Cassette (20 mIU/mL) in Urine, Model/ Part:…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Alere San Diego, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 7, 2026Updated Oct 13, 2026

Brand Name: Expressaire Product Name: DISPOSABLE TOURNIQUET CUFF, 30" X 4" 2-LINE (CS 18) WHITE Model/Catalog Number:…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

ASP Global, LLC.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 7, 2026Updated Oct 13, 2026

EnCor EnCompass Breast Biopsy and Tissue Removal System Console (model number: ENCPCONSOLE) and Driver (model number:…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Bard Peripheral Vascular Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 7, 2026Updated Oct 13, 2026

Systems/units containing affected software/SQL BECKMAN COULTER CHEMISTRY ANALYZER AU480 REF / UDI-DI code: B96692 /…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Beckman Coulter Mishima K.K.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 7, 2026Updated Oct 13, 2026

Presource Packs Containing Stryker StrykeFlow PS and AHTO tube sets: 1) KIT, LAP CHOLE , Catalog Number: PGCGLCBAC; 2)…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Cardinal Health 200, LLC

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 7, 2026Updated Oct 13, 2026

VentStar Resus Neo. Neonatal. 25 Units per Box. Part Number: MP00310 Disposable breathing circuit for use with a…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Draeger, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 7, 2026Updated Oct 13, 2026

HeartSine samaritan PAD (Public Access Defibrillator); HeartSine SAM 350P 350P US Device, US English - 2 Min CPR UDI-DI…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

HeartSine Technologies Ltd.

FDA (openFDA device enforcement)

Food

Reported Oct 7, 2026Updated Oct 13, 2026

Kofinas Garlic Mediterranean Infused Extra Virgin Olive Oil, packaged in 3.4 fl oz (100mL), 8.5 fl oz (250mL), and 17…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Lmsi, LLC

FDA (openFDA food enforcement)

Food

Reported Oct 7, 2026Updated Oct 13, 2026

Organiccs Absolutely Pure, Type-1 Hydrolyzed Collagen Peptides, All-Natural Aid for Strengthening Hair, Skin, Nails,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Pacific Health Sciences LLC

FDA (openFDA food enforcement)

Medical devices

Reported Oct 7, 2026Updated Oct 13, 2026

Computed Tomography X-ray System, Model: uCT 530 with software

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Shanghai United Imaging Healthcare Co., Ltd.

1 more product in this recall

FDA (openFDA device enforcement)

Meat & poultry

Reported Oct 2, 2026Updated Oct 25, 2026

Inexport Logistics LLC Recalls Ineligible Pork Cracklings Products Imported From The Republic of Colombia

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Inexport Logistics LLC

USDA FSIS

Medical devices

Reported Sep 30, 2026Updated Oct 6, 2026

ForeSight Elite Tissue Oximetry Cable REF HEMFSM10 UDI-DI code: 00690103210927 The non-invasive ForeSight oximeter…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Becton, Dickinson and Company

FDA (openFDA device enforcement)

Medical devices

Reported Sep 30, 2026Updated Oct 6, 2026

Presource Convenience Kits: 1) KIT, PRE OP , Catalog Number: AMN548616A; 2) KIT, NICU ADMIT NEW HAN , Catalog Number:…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Cardinal Health 200, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 30, 2026Updated Oct 6, 2026

nGenuity Patient Monitor with Capnography (ETCO2) CAT 8100E1-ST-US, CAT 8100E1-US, CAT 8100EP1, CAT 8100EP1-ST, CAT…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Criticare Technologies, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 23, 2026Updated Sep 29, 2026

Power-Trialysis Short-Term Straight Dialysis Catheter, REF: 5605150; Power-Trialysis Short-Term Straight Dialysis…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Bard Access Systems, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 23, 2026Updated Sep 29, 2026

BD Alaris Pump Infusion Sets 10561554* 10885403232565 50885403232563 BD Alaris Pump Infusion Set, 15 Micron Filter,…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Bd Switzerland Sarl

FDA (openFDA device enforcement)

Food

Reported Sep 23, 2026Updated Sep 29, 2026

PUMPKIN SPICE NO BAKE COOKIE NET WT 3.5 oz. INGREDIENTS: WHOLE GRAIN OATS, MILK, MARGARINE***WATER, SALT, CONTAINS LESS…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Best Friends Bakery, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Sep 23, 2026Updated Sep 29, 2026

Boston Scientific Corporation StoneSmart Connect Console Contents: (1) Power Cord, (1) Power Adaptor, (1)DVI Cable, (1)…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Boston Scientific Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Sep 23, 2026Updated Sep 29, 2026

EWO_02512 (Catalog number 320550) For Investigational Use Only Nano Pro Un-Cannulated Demo Samples Quantity 100

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

embecta Medical II LLC

1 more product in this recall

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.