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 Dec 19, 2018
Laser Fiber Assy-Single Use-LFS-272-RT-0.22NA-SMA905- Slim Extension Sleeve Silver-Sterile ETO- Private label:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leoni Fiber Optics GmbH
4 more products in this recall
FDA (openFDA device enforcement)
Reported Dec 19, 2018
UroLift System REF Catalog Number: UL400-4 Tray Contents: UroLift System with Handle Release Tool STERILE R CE 0050…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Neotract Inc.
FDA (openFDA device enforcement)
Reported Dec 19, 2018
HeartStart MRx, Rechargeable Li-Ion (lithium ion battery), REF: M3538A, which is a component of HeartStart MRx…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America LLC
FDA (openFDA device enforcement)
Reported Dec 19, 2018
St. Jude Medical InfinityTM DBS System 8CH Directional Lead, 30 cm, 0.5 REF 6170 - STERILE EO Rx ONLY CE 0086 0123 St.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.St. Jude Medical, Inc.
FDA (openFDA device enforcement)
Reported Dec 19, 2018
Baraka Hot Curry Powder packed in 7 OZ Plastic Jar
High riskUsing this product could cause serious injury, illness or death — stop using it now.U.B.C. Food Distributors Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Dec 12, 2018
BD BBL Trypticase Soy Agar with 5% Sheep Blood, Catalog No. 221261, (non-selective, non-differential)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Becton Dickinson & Co.
FDA (openFDA device enforcement)
Reported Dec 12, 2018
Captus 3000 Thyroid Uptake System, Model # 5430-0076 and 5430-0077
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Capintec Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Dec 12, 2018
16 count Smartfood Delight Variety Pack Sack
High riskUsing this product could cause serious injury, illness or death — stop using it now.Frito-Lay, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Dec 12, 2018
NEOCONNECT, Enteral Extension with ENFit connector, REF EXT-60NC The NeoMed NeoConnect Enteral Only Extension Set is…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Neomed Inc.
FDA (openFDA device enforcement)
Reported Dec 12, 2018
NOW Vitamin B-50 Complex with C 100 Veg Caps
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.NOW Foods
FDA (openFDA food enforcement)
Reported Dec 12, 2018
Smartypants Kids Complete, Non GMO Multi and omega 3's vitamin D3 for bones, vitamin B12 for Energy: 90 gummies. UPC 8…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smartypants Vitamins
FDA (openFDA food enforcement)
Reported Dec 9, 2018
3-D Meats, LLC Recalls Ready-To-Eat Beef Snack Stick Products due to Misbranding and Undeclared Allergens
High riskUsing this product could cause serious injury, illness or death — stop using it now.3-D Meats, LLC
USDA FSIS
Reported Dec 5, 2018
Ultra Dark Chocolate Amaretto Rainier Cherries, Chukar Cherries brand, packaged in 7.5 oz. plastic pouches. UPC 0 11261…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Chukar Cherry Company
4 more products in this recall
FDA (openFDA food enforcement)
Reported Dec 5, 2018
Sandoz Losartan Potassium and Hydrochlorothiazide Tablets, USP 100 mg/25 mg, 1000-count bottles, Rx Only, Finished Drug…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sandoz, Inc.
FDA (openFDA drug enforcement)
Reported Nov 28, 2018
Ascom Telligence Nurse Call System
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ascom (US) Inc.
FDA (openFDA device enforcement)
Reported Nov 28, 2018
BAZZINI S ROASTED & SALTED IN-SHELL PISTACHIOS SUPER COLOSSAL NATURAL 5 LBS BAG UPC #0 75062 30701 5 THE BAGS ARE RED,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Bazzini LLC
4 more products in this recall
FDA (openFDA food enforcement)
Reported Nov 28, 2018
The SQ-RX Pulse Generator a component of the Subcutaneous Implantable Cardioverter Defibrillator (S-ICD) System The…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
FDA (openFDA device enforcement)
Reported Nov 28, 2018
HOUSE BLEND Barbecue SAUCE INGREDIENTS: ***Contains 2% or less of Soybean Oil***Onion Powder***Calcium Disodium…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Diamond Crystal Brands, Inc.
FDA (openFDA food enforcement)
Reported Nov 28, 2018
Irrisept OR, Finished Bottle Assembly 450 ml STEP 1
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company
FDA (openFDA device enforcement)
Reported Nov 28, 2018
Minicon Clinical Sample Concentrators for In Vitro Diagnostic Use 9031 (Model: Minicon B-15) & 9051 (Model: Minicon…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merck Millipore Ltd.
FDA (openFDA device enforcement)
Reported Nov 28, 2018
PremierPro Aluminum Adjustable Walker
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Svs LLC
FDA (openFDA device enforcement)
Reported Nov 28, 2018
AIA-2000 Analyzer, Model Nos. AIA-2000LA, AIA-2000ST - Product Usage: The AIA-2000 is capable of performing three…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tosoh Bioscience Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Nov 28, 2018
Insulia Diabetes Management Companion
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Voluntis
FDA (openFDA device enforcement)
Reported Nov 28, 2018
Vanguard Knee System -PS Open Box Femoral Left, 62.5 mm Item Number: 183126
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, 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.