All recall categories

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.

Medical devices

Reported May 20, 2026

Brand Name: Dexcom G7 Continuous Glucose Monitoring System Product Name: Dexcom G7 CGM iOS App Model/Catalog Number:…

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

Dexcom, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 20, 2026

Brand Name: DONJOY Product Name: ICEMAN CLASSIC CUBE Model/Catalog Number: 11-0494 Software Version: no Product…

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

Djo, LLC

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 20, 2026

Edwards EVOQUE tricuspid delivery system REF:9850TDS Sterile EO

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

Edwards Lifesciences, LLC

FDA (openFDA device enforcement)

Food

Reported May 20, 2026

Frederik's by meijer Vanilla Bourbon Trail Mix, packed in plastic retail-sized black bag NET WT 9 OZ (255g). On the…

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

Ferris Coffee and Nut Company, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported May 20, 2026

Codman CerebroFlo EVD Catheter with Endexo Technology. Contains 5 sets. Product ID: 37.550.501. The CerebroFlo EVD…

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

Integra LifeSciences Corp. (NeuroSciences)

FDA (openFDA device enforcement)

Medical devices

Reported May 20, 2026

LUCAS 2 Model Number: 99576 Catalog Numbers: 99576-000024 and 99576-000011 UDI-DI code: 00883873904565 LUCAS 3 Model…

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

Jolife AB

FDA (openFDA device enforcement)

Medical devices

Reported May 13, 2026

ERBEFLO CleverCap CO2: Hybrid CO2 Tubing/Cap Set for Olympus Scopes & CO2 Sources, REF: 20325-239; Hybrid CO2…

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

Erbe Medical, LLC

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported May 13, 2026

french broad CHOCOLATE bette's bake sale (a multi-flavor bonbon assortment). 6-piece NET WT. 2.5 OZ (70.75G); 12-piece…

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

French Broad Chocolate Factory

FDA (openFDA food enforcement)

Medical devices

Reported May 13, 2026

Intuitive 8 mm SureForm 30 Gray Reloads Reference Numbers: 48230M-05 and 48230M-06

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

Intuitive Surgical, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported May 13, 2026

LIFEPAK 15, REF: 99577-000025, 99577-000047, 99577-001256, 99577-001217, 99577-001241, 99577-001255, 99577-001219,…

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

Physio-Control, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported May 6, 2026

Brand Name: HiResolution" Bionic Ear System Product Name: M Zn-Air Battery Pak Model/Catalog Number: CI-5501-110;…

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

Advanced Bionics, LLC

FDA (openFDA device enforcement)

Medical devices

Reported May 6, 2026

Brand Name: Kiwi Omni Vacuum Delivery System Product Name: Kiwi Omni Vacuum Delivery System Model/Catalog Number:…

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

Clinical Innovations, LLC

FDA (openFDA device enforcement)

Medical devices

Reported May 6, 2026

Brand Name: Disposable Mixing Bowls with Spatula Product Name: Mixing Bowl and Spatula Model/Catalog Number:…

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

Zimmer, Inc.

FDA (openFDA device enforcement)

Food

Reported Apr 29, 2026

CHIPS AHOY! Baked Bites Brookie .22.4 oz Carton ( 2.8 oz pouch ) and 7.7 oz Carton ( 1.4 oz pouch)

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

Mondelez Global LLC

FDA (openFDA food enforcement)

Medical devices

Reported Apr 22, 2026

Cytal Wound Matrix 2-Layer 5x5 cm. Product ID: WSM0505.

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

Integra LifeSciences Corp. (NeuroSciences)

4 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Apr 22, 2026

Instinct Plus Endoscopic Clipping Device REF: G58010 Rx Only, Sterile EO

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

Wilson-Cook Medical Inc.

FDA (openFDA device enforcement)

Food

Reported Apr 15, 2026

Vital Nutrients Aller-C (vitamin C, citrus bioflavonoids, isoquercitrin, and bromelain)100 count bottles and 200 count…

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

Blueroot Health, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 15, 2026

Stryker Sustainability Solution Color Cuff 24" (Yellow) Quick Connect Dual Port Single Bladder REF 5921-024-235 Stryker…

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

Stryker Sustainability Solutions

FDA (openFDA device enforcement)

Medical devices

Reported Apr 15, 2026

Tornier HRS Max parts: 1. TORNIER HRS Max Tuberosity Body Lat Coat, Small, Cat. No. ARS1041101 2. TORNIER HRS Max…

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

Tornier, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Apr 8, 2026

Brand Name: da Vinci S, Si Monopolar Curved Scissors Instrument Product Name: da Vinci S and Si Monopolar Curved…

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

Intuitive Surgical, Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Apr 8, 2026

" Dumpling Vegetable 4.5 oz 011110658067 " Loaded Dumpling Vegetable 5.7 oz 011110696953

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

Jfe Franchising Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Apr 8, 2026

MiniMed 670G Insulin Pump (MMT-1760, MMT-1761, MMT-1762, MMT-1780, MMT-1781, MMT-1782)

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

Medtronic MiniMed, Inc.

13 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Apr 8, 2026

Divided Sunset Multi Collagen Peptides, 8 Ounce, Stand-up Pouch, UPC Code: 8 50005 60689 5

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

Tg Foods Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Apr 8, 2026

Jiffy Original Composite Polisher Cups (Coarse) 12pk, REF 7011.

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

Ultradent Products, 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.