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

Food

Reported Mar 13, 2019

Big Daddy s Bold Cheese Pizza, item No. 78985. 3-Pack. Contains 9-44.53 oz. Pizzas. Net Wt. 25.04 Lbs. (11.36 kg) For…

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

Schwan's Global Supply Chain, Inc., Specialy Foods Plant

FDA (openFDA food enforcement)

Medical devices

Reported Mar 13, 2019

Stryker Sustainability Solutions (SSS) reprocessed Arthroscopic Shavers Arthroscopic shavers can be used to abrade, cut…

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

Stryker Sustainability Solutions

FDA (openFDA device enforcement)

Drugs

Reported Mar 13, 2019

Topical Solution USP Hydrogen Peroxide First Aid Antiseptic Oral Debriding Agent 32 Fl. Oz. (1 QT) 946 mL bottle,…

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

Vi-Jon, Inc.

FDA (openFDA drug enforcement)

Medical devices

Reported Mar 6, 2019

Alcon or Endure Ophthalmic Microscope Product Usage: Used for low magnification visualization during ophthalmic…

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

Alcon Research Laboratories Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 6, 2019

Phoenix AST-s Indicator, Catalog Number 246009

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

Becton Dickinson & Co.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 6, 2019

Entuit Secure Gastrointestinal Suture Anchor Set, Catalog Number GIAS-SRM-2, Order Number G35569 The Entuit Secure…

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

Cook Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Mar 6, 2019

Equinoxe Preserve Humeral Stem, 8mm Product Usage: The Equinoxe Preserve Stems are indicated for use in skeletally…

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

Exactech, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 6, 2019

icumedical ChemoLock Vial Spike, 20mm, REF CL-80S The ChemoLock Closed System Drug Transfer Device prevents the…

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

ICU Medical, Inc.

FDA (openFDA device enforcement)

Food

Reported Mar 6, 2019

Montmorency Tart Cherry Concentrate 100% Juice 32-oz bottle (sold individual and 12 per case), 16-oz bottle (sold…

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

King Orchards

FDA (openFDA food enforcement)

Medical devices

Reported Mar 6, 2019

The WinStation Retinal Imager, also known as Merge Eye Station. DCF-1024 & DCF-512 Digital Imaging System Product…

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

Merge Healthcare, Inc.

FDA (openFDA device enforcement)

Food

Reported Mar 6, 2019

Produce Packaging, Inc. Cauliflower, Rice 6/11 oz

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

Produce Packaging Inc.

21 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Mar 6, 2019

Tegral Satin Gold CL Cr¿me Cake, packaged in 50 lb. bag.

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

Puratos Corporation

FDA (openFDA food enforcement)

Medical devices

Reported Mar 6, 2019

BRANSIST safire Product Usage: DIGITAL ANGIOGRAPHY SYSTEM This system is intended to be used for radiologic…

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

Shimadzu Medical Systems USA Com

FDA (openFDA device enforcement)

Medical devices

Reported Mar 6, 2019

Vitality¿ Spinal Fixation System. Thoracolumbosacral pedicle screw system (non-sterile). Pedicle screw fixation is…

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

Zimmer Biomet Spine Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 27, 2019

AMIA Automated Peritoneal Dialysis System Product Usage: It is intended for automatic control of dialysate solution…

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

Baxter Healthcare Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 27, 2019

Stingray" Guidewire, labeled as 300cm. intended to facilitate placement of balloon dilatation catheters or other…

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

Boston Scientific Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Feb 27, 2019

TRINIAS for diagnostic imaging and interventional procedures in cardiac angiography, neurovascular angiography,…

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

Shimadzu Medical Systems USA Com

FDA (openFDA device enforcement)

Medical devices

Reported Feb 20, 2019

COBRA FUSION 50, Ablation System, Catalog # (REF) 700-002

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

AtriCure, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 20, 2019

Coconut Chocolate RXBARs , 1.83 oz., single bar, , 12-count carton, 5-count carton, 4-count carton

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

Chicago Bar Company LLC Rxbar

18 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 20, 2019

Hemotherm CE Dual Reservoir Cooler/Heater, Model No. 400CE Product Usage: The HEMOTHERM¿ Model 400CE Dual Reservoir…

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

Cincinnati Sub-Zero Products LLC, a Gentherm Company

FDA (openFDA device enforcement)

Food

Reported Feb 20, 2019

Culinary Secrets, Butterscotch Instant Pudding Mix, Net Wt. 28 OZ, Marketed by Independent Marketing Alliance, Houston,…

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

Diamond Crystal Brands, Inc.

10 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 20, 2019

MOSAIQ¿ Oncology Information System and Sequencer MOSAIQ is an oncology information system used to manage workflows for…

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

Elekta, Inc.

FDA (openFDA device enforcement)

Food

Reported Feb 20, 2019

Organic Sunflower Butter, Net Wt. 16 oz. (453g) Packaged under the following brand names: 1. Thrive Market, UPC…

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

Oskri Corp.

19 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Feb 20, 2019

Parent's Choice Toddler Next Stage¿ Milk Drink Powder Natural Milk Flavor With Other Natural Flavors, Stage 3, 1 Year…

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

PBM Nutritionals, LLC

FDA (openFDA food 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.