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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 48,122 notices were distributed nationwide, so they reach Kentucky too — those are in the archive.

Medical devices

Reported Mar 11, 2020

Elecsys CA 19-9, Cat. No. 07027028190 - Product Usage: the product is an immunoassay for monitoring and management of…

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

Roche Diagnostics Operations, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 11, 2020

Seca 402/403 Baby Scale Cart, Ref # 4020000009/ REF # 4030000009

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

Seca

FDA (openFDA device enforcement)

Food

Reported Mar 11, 2020

Chocolate Fudge Mini Bundt Cake sold by the slice packaged in Self Serve and Plastic clam shell containers PLU 21287

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

Whole Foods Market

3 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Mar 4, 2020

C&H Pure Cane Sugar Golden Brown, 32 oz (2 LB) plastic bag, UPC 015800090038, Lots 50042 (Best By Jan 21, 2022) & 50043…

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

Domino Foods Inc.

7 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Mar 4, 2020

Coburn Farms Snackers, Sharp Yellow Cheddar Cheese, Cherry Juice Infused Dried Cranberries & Roasted Sea Salted…

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

Great Lakes Cheese Co. Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Mar 4, 2020

Ellipse, Tiered-therapy Cardioverter/Defibrillator, REF (UDI/GTIN): CD1377-36QC (05414734507646), CD2411-36C…

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

St Jude Medical, Cardiac Rhythm Management Division

FDA (openFDA device enforcement)

Food

Reported Feb 26, 2020

Taspen's Organics Breathe Easy Herbal Tincture Dietary Supplement, sold in 1 oz, 2 oz, and 4 oz amber glass bottles…

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

Green Water, LLC

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 26, 2020

SnapLink, Ref Part No. 438-2190, L6R SnapLink, Slot .022, TQ--28, Ang +2, Rot +2, Qty 10, Made in Mexico, CE 0086, Rx…

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

Ormco/Sybronendo

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 26, 2020

OPTILITE IgM Kit, REF: NK012.OPT.A, IVD, UDI: 05051700017565

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

The Binding Site Group, Ltd.

FDA (openFDA device enforcement)

Food

Reported Feb 19, 2020

bliss anti-stress formula Dietary Supplement, 60 Tablets; Manufactured For and distributed by: Market America, Inc.,…

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

Market America Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Feb 19, 2020

Medtronic MiniMed 630G System with SmartGuard, Ref/Model # MMT-1515, MMT-1715, MMT-1714, MMT-1754, and MMT-1755 *US and…

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

Medtronic Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 19, 2020

Stratum Lapidus Plate - Small Rt, Part No. STRM-LAP-SMR, UDI 00817701025467. The product is part of the Stratum Foot…

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

Nextremity Solutions

FDA (openFDA device enforcement)

Medical devices

Reported Feb 19, 2020

Button-Style Tocotransducer (Nautilus), 8-foot Cord 2264HAX, that may have been serviced with the following: Pacific…

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

Pacific Medical Group Inc.

9 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 19, 2020

Revanesse Versa, PN40081

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

Prollenium Medical Technologies Inc.

FDA (openFDA device enforcement)

Food

Reported Feb 19, 2020

Ready Pac Bistro - Spinach Dijon Salad with Sweet Onion Dijon Vinaigrette; Baby Spinach, Hard Boiled Eggs, Monterey…

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

Ready Pac Foods, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Feb 19, 2020

cobas infinity core, Material No. 7154003001. The device is a calculator/data processing module, for clinical use.

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

Roche Diagnostics Operations, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 19, 2020

Stryker, Omega 4.75 mm,. PEEK Knotless Anchor System, Double-Double, REF 3910-500-472, UDI 07613327464832, Sterile R,…

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)

Food

Reported Feb 12, 2020

Bulk Pail Product -- Almark Foods HARD COOKED BROKEN EGG WHITES 20 LB pail, DIST BY: ALMARK FOODS, GAINESVILLE, GA…

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

Almark Foods, LLC

28 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 12, 2020

Reinforced Introducer Sets Maquet 7 Fr., Part Number: 0684 00 0403 06. It is an accessory to be used for percutaneous…

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

Datascope Corporation

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 12, 2020

Garlic Parmesan Sauce; DP# 4478 FG# 02620 8/16 fl. oz (4.73 ml) pouches; NET WT. 8.05 lbs (3.65 kg) Produced for…

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

Golden State Foods

3 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 12, 2020

da Vinci Xi Surgical System Surgical System, IS4000, 00886874114216 - Product Usage: used with an endoscope, surgical…

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

Intuitive Surgical, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 12, 2020

Fresh Grab Ham & Swiss on Pretzel Sub Bun, 6 oz., UPC: 612510001028

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

Lipari Foods Operating Company, LLC.

31 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 12, 2020

Pacific Medical GE Corometrics Nautilus Toco Transducer w/knob, 2264HAX, FFCM3205

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

Pacific Medical Group Inc.

6 more products in this recall

FDA (openFDA device enforcement)

Drugs

Reported Feb 12, 2020

ranitidine hydrochloride, USP ,150 mg tablets a) 14-count bottles ( NDC 43063-844-14); b) 30-count bottles (NDC…

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

PD-Rx Pharmaceuticals, Inc.

FDA (openFDA drug 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.