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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.

3,340 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 Aug 20, 2025

Description/REF: BD PYXIS MEDBANK MINI 1FH-1FM/169-137, BD PYXIS MEDBANK MINI 4HM/169-113, BD PYXIS MEDBANK MINI…

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

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 20, 2025

Clover Valley Instant Coffee, NET WT 8 OZ (227 g), packaged in a glass jar, packed 6 jars per case, UPC: 876941004069,…

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

Dollar General Corporation

FDA (openFDA food enforcement)

Medical devices

Reported Aug 20, 2025

High Pressure Tubing: REF: 502211002, HP9720E/C, HP9721E/C

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

Merit Medical Systems, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Aug 20, 2025

Signature Cafe Premium Tuna Salad, net wt. 3lb (48oz). Foodservice item to be used by deli. Product is packaged in…

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

Reser's Fine Foods, Inc.

6 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 20, 2025

Brand Name: PERLA ¿ TL MIS Product Name: CANNULATED FENESTRATED POLYAXIAL SCREW Model/Catalog Number: MPF-PS 65 40-S…

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

Spineart Sa

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 20, 2025

Brand Name: HeartMate Product Name: Mobile Power Unit, AC Power Cord Model/Catalog Number: 107760 Software Version: N/A…

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

Thoratec LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 13, 2025

BD Alaris Pump Module Model, 8100 with Guardrails, Suite MX software versions

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

CareFusion 303, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Aug 13, 2025

Favorite Day Bakery Frosted Sugar Cookies, 10 count, Net Wt 13.5 oz (383g). UPC - 85239-41250 3. Dist. By Target…

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

Give and Go Prepared Foods Corp.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 6, 2025

HeartSine SAM 350P, HeartSine SAM 360P, and HeartSine SAM 450P The HeartSine samaritan¿ PAD (Public Access…

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

HeartSine Technologies Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 6, 2025

IontoPatch STAT, On-the-Go Patch Therapy, Model/Catalog Number D-0062-080; IontoPatch is an Iontophoresis transdermal…

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

LTS Therapy Systems, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 6, 2025

Inseego USB8 4G Dongle Kit, Part Number: 01-2298, which contains USB Flash Drive, Part Number: 43-2011. The kit is an…

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

Remote Diagnostic Technologies Ltd.

FDA (openFDA device enforcement)

Food

Reported Aug 6, 2025

Sheehan Brothers Vending Cheeseburger, 4.7 oz (132g), individually wrapped in plastic, UPC: 100000952375

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

Sheehan Brothers Vending

5 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 6, 2025

Volcano Visions Digital IVUS Catheter: PV.014P (Platinum), REF:85910P; PV.014P RX, REF: 014R; and PV.018, REF: 86700,…

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

Volcano Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 30, 2025

HSG Procedure Tray. Model Number: 6050T. The HSG Procedure Tray is for use in hysterosalpingography and…

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

CooperSurgical, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 30, 2025

Covidien Nellcor Bedside SpO2 Patient Monitoring System: REF: PM100N, 10005941, DLPM100N, DL10005941, DSPM100N,…

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

Covidien

FDA (openFDA device enforcement)

Medical devices

Reported Jul 30, 2025

ACUVUE¿ OASYS MAX 1-Day MULTIFOCAL

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

Johnson & Johnson Vision Care, Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 30, 2025

Artisan Style 1/2 Loaf, Net wt. 12 oz (340g) 024126018152 1/2 Loaf of white bread with white flour topping and two…

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

Lewis Bakeries

FDA (openFDA food enforcement)

Food

Reported Jul 30, 2025

Ritz Peanut Butter Cracker Sandwiches, Net Wt.27.6 oz, 20 count (20x1.38 oz) 6- pack of cracker sandwiches inside…

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

Mondelez Global LLC

3 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Jul 30, 2025

Azurion 7 M20. Fluoroscopic X-Ray System.

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

Philips Medical Systems Nederland B.v.

FDA (openFDA device enforcement)

Medical devices

Reported Jul 30, 2025

Stryker, StrykeFlow , REF: 0250070500, 2, Disposable Suction/Irrigator without Disposable Tip

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

Stryker Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Jul 23, 2025

SwabCap Disinfecting Cap for Needlefree Connectors: SwabSleeve, REF: SCXT3-5-2000; SwabCap, 200-ct. Box, REF: SCXT3-2000

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

ICU Medical, Inc.

FDA (openFDA device enforcement)

Food

Reported Jul 23, 2025

J. Higgs Potato Chip Mix, 18 1oz singles, net weight 180z., UPC 0-51933-37327-3

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

Saratoga Potato Chips LLC

FDA (openFDA food enforcement)

Food

Reported Jul 23, 2025

Wei-Chuan branded Black Fungus Slice. Net weight: 2.5 oz UPC#: 072869231321

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

Wei-Chuan USA Inc.

FDA (openFDA food enforcement)

Food

Reported Jul 23, 2025

Dubai emek SPREAD PISTACHIO CACAO CREAM WITH KADAYIF NET WT. 9.7oz UPC 8 69652 10130 1 Manufacturer: Emek Dogal Saglik…

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

World Market Management Services, LLC

FDA (openFDA food 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.