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.
Reported Sep 7, 2022
Metalogix Self-Drill Half-Pin, a component of the Revolution External Fixation System. Orthopedic. Metalogix Self-Drill…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.New Standard Device Inc.
FDA (openFDA device enforcement)
Reported Sep 7, 2022
Pentacam AXL Wave REF 70020. Used to image the anterior segment of the eye.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Oculus Optikgeraete GmbH
2 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 7, 2022
Lemon Dill Butter Pucks
High riskUsing this product could cause serious injury, illness or death — stop using it now.Raw Seafoods Inc.
FDA (openFDA food enforcement)
Reported Sep 7, 2022
Woodland Ingredients X06D Arborio Rice, 25 lbs. bag UPC 00687080007374 Woodland Ingredients X16D Italian Arborio Rice,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Woodland Foods LLC
FDA (openFDA food enforcement)
Reported Sep 7, 2022
Priyems Sambar Spicy Lentil Soup 800 grams (1.76 lbs) UPC 8 61754 00010 0, 8 retail units per wholesale case, Frozen
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Yem Foods LLC
3 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 31, 2022
NUCLISENS easyMAG Magnetic Silica, REF 280133, 24 x 1.2mL bottles/kit.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.bioMerieux, Inc.
FDA (openFDA device enforcement)
Reported Aug 31, 2022
(1) GE Centricity Universal Viewer 6.0, Model 2088026-9XX; (2) GE Centricity Universal Viewer 7.0, Model 5826659-0XX;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
FDA (openFDA device enforcement)
Reported Aug 31, 2022
INTERA 3000 Hepatic Artery Infusion Pump, 30 mL, Sterile, Rx Only. implantable infusion pump.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Intera Oncology, Inc.
FDA (openFDA device enforcement)
Reported Aug 31, 2022
Vanta Clinician Programmer Application, Model A71200. For programming of the Medtronic Model 977006 Vanta implantable…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Neuromodulation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 31, 2022
Homemade Bofrot/Puff Puff mix, Pegroks Kitchen 24 ounce packages - 12 packages per case packaged in purple mylar bags
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pegroks Kitchen
FDA (openFDA food enforcement)
Reported Aug 31, 2022
NeuRx Diaphragm Pacing System (NeuRx DPS) External Pulse Generator (EPG), Part No. 23-0021.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Synapse Biomedical Inc.
FDA (openFDA device enforcement)
Reported Aug 24, 2022
Power electronic box, Part #AS-0066, subassembly for the MyoCycle MC-2.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Myolyn Inc.
FDA (openFDA device enforcement)
Reported Aug 17, 2022
The Cholestech LDX¿ System combines enzymatic methodology and solidphase technology to measure total cholesterol, HDL…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alere San Diego, Inc.
FDA (openFDA device enforcement)
Reported Aug 17, 2022
Big Olaf, Frozen Ice Cream to include all flavors, sold in sizes 2.5 gal, 1/2 gal, and pints packaged in plastic…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Big Olaf Creamery LLC dba Big Olaf
FDA (openFDA food enforcement)
Reported Aug 17, 2022
Clear American brand "Strawberry Punch Snow Cone" flavored sparkling water beverage with other natural flavors; 1-liter…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Refresco Beverages US Inc.
FDA (openFDA food enforcement)
Reported Aug 17, 2022
cobas e801 Immunoassay Analyzer
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
FDA (openFDA device enforcement)
Reported Aug 17, 2022
Xhibit Telemetry Receiver, Model: 96280
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spacelabs Healthcare, Inc.
FDA (openFDA device enforcement)
Reported Aug 17, 2022
Azacitidine for Injection 100mg/vial Lyophilized Powder, Rx Only, Mfd. in Romania By: Sindan Pharma SRL For BluePoint…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Teva Pharmaceuticals USA Inc.
FDA (openFDA drug enforcement)
Reported Aug 10, 2022
PRESTIGE ATRAUMATIC GRASPER W/PORT DUAL ACTION, ROTATING 5mm DIAM., 36cm LENGTH. Product Code 8360-10
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Aesculap Implant Systems LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 10, 2022
EkoSonic Kit 135cm, 12cm TZ The EkoSonic Endovascular Device is packaged as a kit that includes both the USC and IC…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 10, 2022
The E-100 Generator (PN 374848-09) is a bipolar electrosurgical unit (ESU) designed to be used with the da Vinci Xi and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
FDA (openFDA device enforcement)
Reported Aug 10, 2022
UroLift System REF UL400-4, QTY 4 Urolfit System with Handle Release Tool
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Neotract Inc.
FDA (openFDA device enforcement)
Reported Aug 10, 2022
SARS CoV 2 rapid antigen test kits packaged under the following brands: Oral Rapid Test, Oral Rapid Antigen Test, SML…
High riskUsing this product could cause serious injury, illness or death — stop using it now.North American Diagnostics
FDA (openFDA device enforcement)
Reported Aug 10, 2022
Merlin PCS 3650 programmer Model 3330 software
Moderate riskThis product could cause temporary or reversible health problems — stop using it.St. Jude Medical, Cardiac Rhythm Management Division
2 more products 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.