All recall categories

Recalls distributed in Ohio

These notices name Ohio 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.

5,400 stored notices name Ohio, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Ohio too — those are in the archive.

Medical devices

Reported Nov 6, 2024

LIFEPAK 15 (LP15) Model/Catalog Numbers: o 97577-000101 o 99577-000046 o 99577-000055 o 99577-000061 o 99577-000076 o…

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

Physio-Control, Inc.

FDA (openFDA device enforcement)

Food

Reported Nov 6, 2024

Item 407118, UPC 13454 38493, Bistro 28 Creamy Green Chile Chicken Enchilada Express Meal Kit. Make 6 Enchiladas. Ready…

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

Reser's Fine Foods, Inc.

17 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 6, 2024

Brand Name: Vial2Bag Advanced¿ Product Name: Vial2Bag Advanced¿ 20mm Admixture Device Model/Catalog Number: 6070030…

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

West Pharmaceutical Services AZ, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 6, 2024

1) Flex Extenders, 5.2" x 15mm OD x 15mm ID REF S6411P 2) Flex Extender, 5.2" x 15mm OD x 22/15mm ID REF 7 5132 The…

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

Westmed, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2024

AD-TECH Spencer Probe Depth Electrode, REF SD04R-AP58X-000 4-Contact 1.12mm (A style) Depth Electrode

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

Ad-Tech Medical Instrument Corporation

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2024

Boston Scientific myLUX Patient Application for an Apple Mobile device, Model Number 2939, Version 2.0.101, 2.0.110,…

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

Boston Scientific Corporation

FDA (openFDA device enforcement)

Food

Reported Oct 30, 2024

Lactaid Lactose Reduced milk 1. 96 oz Lactaid Whole Milk 2. 96 oz Lactaid 2% Milk 3. 96oz Lactaid 1% Milk 4. 96oz…

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

HP Hood LLC

FDA (openFDA food enforcement)

Medical devices

Reported Oct 30, 2024

STERILIZABLE INTERNAL DEFIBRILLATION PADDLES REF LP20 STERILIZABLE INTERNAL DEFIBRILLATION PADDLES REF LP15…

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

Physio-Control, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2024

Trinias unity, Digital Angiography System with Catheterization Table, Model: KS-100 This system consists of the…

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

Shimadzu Corporation Medical Systems Division

FDA (openFDA device enforcement)

Medical devices

Reported Oct 30, 2024

Quantum Perfusion Systems for CPB, Roller Pumps use peristaltic action to propel blood through the venous and arterial…

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

Spectrum Medical Ltd.

FDA (openFDA device enforcement)

Food

Reported Oct 30, 2024

Happy Moose Juice Tropical Roots packaged in a plastic 12 fl. oz. bottle. Ingredients: Mandarin Orange, Organic Carrot…

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

Youngstown Grape Distributors, Inc.

4 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Oct 23, 2024

IMMAGE Immunochemistry Systems IGM Immunoglobulin M Reagent REF 447610 IGM reagent, when used in conjunction with…

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

Beckman Coulter Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 23, 2024

KINOVA Jaco assistive robot. Model Numbers: PJ 0000 0001, PJ 0000 0012, PJ 0090 0001, PJ 0090 0006, KR MJ2 0001. Jaco…

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

Kinova Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 23, 2024

Monarch Inflation Device 30 atm/bar REF IN2130 Injector And Syringe, Angiographic/Syringe, Balloon Inflation - The 30…

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

Merit Medical Systems, Inc.

15 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 23, 2024

Brand Name: NOVA ORTHO-MED INC. Product Name: MONARCH ROLLATOR BLUE Model/Catalog Number: 4329BL Product Description:…

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

Nova Ortho-Med Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Oct 23, 2024

S'mores Bites, 1 yummy pound, Distributed by Nuts.com, Cranford, NJ, 07016

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

Nuts.com

FDA (openFDA food enforcement)

Medical devices

Reported Oct 23, 2024

Cortera Spinal Fixation System Screw, Poly, Solid, 6.5mm x 45mm, REF: 150100-65045

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

XTANT Medical Holdings, Inc.

FDA (openFDA device enforcement)

Drugs

Reported Oct 23, 2024

First Aid Antiseptic Ointment, Povidone Iodine USP 10%, Inactive Ingredients: mineral oil, petrolatum. NET Wt. 1 OZ…

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

Zhejiang Jingwei Pharmaceutical Co., Ltd.

FDA (openFDA drug enforcement)

Medical devices

Reported Oct 16, 2024

iCast Covered Stent, 6MMx16MMx120CM, Model Number 42616

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

Atrium Medical Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Oct 16, 2024

Monarch Platform (Endoscopy), REF: MON-000005-01, MON-000005-01R. Monarch Platform (Bronchoscopy), REF: MON-000006,…

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

Auris Health Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Oct 16, 2024

Minute Maid Zero Sugar Lemonade 12 cans carton UPC 0 25000 12115 9 CANNED UNDER THE AUTHORITY OF THE COCA-COLA COMPANY,…

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

COCA COLA Consolidated LLC

FDA (openFDA food enforcement)

Medical devices

Reported Oct 16, 2024

Triathlon Universal TS Baseplate Size 2 - A single use sterile implantable device intended for cemented applications…

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

Howmedica Osteonics Corp.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Oct 16, 2024

MEDIHONEY Dressing with Active Leptospermum Honey Wound and Burn Dressing W/APPLICATOR, 1.5oz tube (Model Number 31515)…

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

Integra LifeSciences Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Oct 16, 2024

NxTAG Respiratory Pathogen Panel, REF: I051C0447

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

Luminex Molecular Diagnostics Inc.

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.