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.
Reported Oct 7, 2020
WILD MUSHROOM BARLEY soup; Manufactured By: Hale & Hearty Soups; 2x9.6lbs; 13.8 net weight; Keep Refrigerated
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hale And Hearty Soups, LLC
FDA (openFDA food enforcement)
Reported Oct 7, 2020
Stryker IsoAir 2.0 support surface-provides pressure redistribution and is intended to assist in management of the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Medical Division
FDA (openFDA device enforcement)
Reported Sep 30, 2020
Speed Stitch Needle Cassette
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ArthroCare Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 30, 2020
DxA 5000; Catalog Number:B50516; UDI:15099590707118 - Product Usage: The DxA 5000 is a high-speed, modular, automated…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Biomedical GmbH
FDA (openFDA device enforcement)
Reported Sep 30, 2020
BECKMAN COULTER ACCESS Immunoassay Systems - Access Unconjugated Estriol, REF 33570.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter Inc.
FDA (openFDA device enforcement)
Reported Sep 30, 2020
BioPlex 2200 Syphilis Total & RPR Linked Immunoabsorption Assay, Treponema pallidum:UDI:03610520653012 - Product Usage:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bio-Rad Laboratories, Inc.
FDA (openFDA device enforcement)
Reported Sep 30, 2020
NM/CT 850 Model Number: H3907AD
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare, LLC
7 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 30, 2020
Lightly salted microwave popcorn packaged in the following ways: 1) Cadia Organic Lightly Salted Popcorn, Net Wt. 9.9…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Gilster-Mary Lee Corp.
4 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 30, 2020
Perceval Single Use Accessory Kit, Size S, REF: ICV1345, Sterile EO, Rx Only, CE, UDI: 8022057015204 - Product Usage:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sorin Group Italia S.r.l.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 30, 2020
EVOLVE STEM 8.5MM Model # 496S085
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Wright Medical Technology Inc.
FDA (openFDA device enforcement)
Reported Sep 23, 2020
Spicy Beef & Vegetables with Rice & Sesame Seeds meal kits containing onions delivered the week of July 27, 2020.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Blue Apron Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 23, 2020
Coolhaus Awesome Ice Cream -That Dough Though Ice Cream Sandwich; Chocolate chip cookies, cookie dough batter with gobs…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Coolhaus
FDA (openFDA food enforcement)
Reported Sep 23, 2020
Herr s GameDay Tailgate Tacos Flavored Potato Chips 6.5 oz. packaged in a flexible metalized bag. UPC Code: 7260006434
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Herr Foods Inc.
FDA (openFDA food enforcement)
Reported Sep 23, 2020
FlexLab (FLX) with Sysmex XN-9000/XN-9100 Interface Module (dual robot) FLX-290-10; FLX-290-20 and Track to Rack Module…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Inpeco S.A.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 23, 2020
The TaqPath RT-PCR COVID-19 Kit with Applied Biosystem's COVID-19 Interpretive Software v1.2 for 7500 RTPCR…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Life Technologies Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 23, 2020
Maquet/Getinge Rotaflow System Console US (115 V / 60 Hz) - Product Usage: Instructions for Use - Centrifugal Pump…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Maquet Cardiovascular US Sales, LLC
FDA (openFDA device enforcement)
Reported Sep 23, 2020
NovaPACS Diagnostic Viewer. NovaPACS is a picture archiving and communication system software that retrieves,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Novarad Corporation
FDA (openFDA device enforcement)
Reported Sep 23, 2020
Model No:T-SPOT.TB8, Catalogue No.: TB.300; UDI: 1505171600030 - Product Usage: intended for use as an aid in the…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Oxford Immunotec
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 16, 2020
BD Alaris System; Alaris Syringe Module Model 8110; BD Alaris System; Alaris PCA Module Model 8120; BD Alaris System;…
High riskUsing this product could cause serious injury, illness or death — stop using it now.CareFusion 303, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 16, 2020
Various HelloFresh and EveryPlate meal kits containing onions received by consumers from June 25 through July 31, 2020.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hellofresh US
FDA (openFDA food enforcement)
Reported Sep 16, 2020
Ion Catheter Reprocessing Cover, IF1000 (Part Number:490114-02) UDI:00886874116845.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 16, 2020
Medcomp 15.SF X 24CM Titan HD CATHETER (CUFF 19CM FROM TIP) Ref: THD155024
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medical Components, Inc. dba MedComp
FDA (openFDA device enforcement)
Reported Sep 16, 2020
Merge PACS
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merge Healthcare, Inc.
FDA (openFDA device enforcement)
Reported Sep 16, 2020
PROFEMUR Titanium and Cobalt Chrome modular necks, Item Numbers and descriptions: Item Number Description Description 2…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.MicroPort Orthopedics Inc.
FDA (openFDA device 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.