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 Jul 8, 2026
Pepperoni Rolls, Net Wt. 5 oz (141g), individually packaged in a clear plastic bag, UPC 601959803041
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fry Pie Factory LLC
FDA (openFDA food enforcement)
Reported Jul 8, 2026
Breathing circuit set, coaxial: REF: 260127, 260128, 260167, 260168 used with HAMILTON-C1, HAMILTON-T1 and HAMILTON-MR1…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Hamilton Medical AG
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 8, 2026Updated Sep 16, 2026
Oribe Serene Scalp Densifying Shampoo, packaged in 8.5 fl. oz. (250 mL) bottles with UPC 840035231242 and 33.8 fl. oz.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.KAO USA Inc.
FDA (weekly enforcement report)
Reported Jul 8, 2026
MorningStar Farms Buffalo Chik'n Nuggets, 100% Plant Protein Vegan Nuggets, Net Wt. 10.5 oz. (298g), packaged in a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mars Snacking
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jul 8, 2026
Radius VSM ECG pre-connected Set, REF: 4842, 4695
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Masimo Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 8, 2026
Brand Name: Pilling Wecksorb Product Name: Pilling Wecksorb Neurosponges (Cotton) Pilling¿ Wecksorb Neurosponge Strips…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex LLC
FDA (openFDA device enforcement)
Reported Jul 8, 2026
GORE¿ TAG¿ Thoracic Branch Endoprosthesis Side Branch Component Catalog Numbers (by Region) United States (includes…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.W L Gore & Associates, Inc.
FDA (openFDA device enforcement)
Reported Jul 1, 2026Updated Sep 16, 2026
Determine HIV 1/2 Ag/Ab Combo 25T, Model/Catalog No. 7D2648
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Diagnostics Scarborough, Inc.
FDA (weekly enforcement report)
Reported Jul 1, 2026
Acumed Hexalob Screw various sizes: REF Numbers: : 3070-27008 2.7mm x 8mm NL Hexalobe Screw; 3070-27009 2.7mm x 9mm NL…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Acumed LLC
FDA (openFDA device enforcement)
Reported Jul 1, 2026
Intera Oncology INTERA 3000 Hepatic Artery Infusion Pump, AP-0300H, implantable drug delivery device
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
FDA (openFDA device enforcement)
Reported Jul 1, 2026
6/11oz Sunflower Seeds Salted
High riskUsing this product could cause serious injury, illness or death — stop using it now.George J Howe Company, Inc.
5 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 1, 2026
Da Vinci ASSY, PSS, SP1098, Part Number: 380601
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intuitive Surgical, Inc.
FDA (openFDA device enforcement)
Reported Jul 1, 2026
INZONE DETACHMENT SYSTEM, REF: M00345100950
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Neurovascular
FDA (openFDA device enforcement)
Reported Jul 1, 2026
1.5oz Zapp's Bayou Blackened Ranch Kettle Chips, Plastic Bag.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Utz Quality Foods, LLC
5 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 24, 2026
directCHECK ACT-LR whole blood quality control, level 2 Model/Catalog Number: DCGLR-2
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Accriva Diagnostics, Inc.
FDA (openFDA device enforcement)
Reported Jun 24, 2026
Ritmed Neurological Sponges, Description/REF: 0.5x0.5in, Non-Sterile/55992C; 0.5x1.0in, Non-Sterile/55993C; 0.5x3.0in,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.AMD Medicom Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 24, 2026
PARACENTESIS KIT, REF: AK-00376, ASK-00376-VCU
High riskUsing this product could cause serious injury, illness or death — stop using it now.Arrow International, LLC
34 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 24, 2026
BD Connecta" BD Luer-Lok" 360 REF 394910 UDI-DI code: 00382903949106 BD Connecta" Stopcocks are used to administer…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bd Switzerland Sarl
FDA (openFDA device enforcement)
Reported Jun 24, 2026
iLet Bionic Pancreas, REF: BB1001
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beta Bionics, Inc.
FDA (openFDA device enforcement)
Reported Jun 24, 2026
Splashwire Hydrophilic Guide Wire: REF: MSWSTDA35150 UDI-DI codes: 00884450529645 00884450529669 00884450529690 REF:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merit Medical Systems, Inc.
FDA (openFDA device enforcement)
Reported Jun 24, 2026
Mito Red Light, Super Mobile
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mito Red Light Inc.
FDA (openFDA device enforcement)
Reported Jun 24, 2026
Nutrisystem, Chocolate Cheesecake, 2 oz (57g) packages, Flow Wrapped, 48 units per case, Keep frozen
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Nutrisystem Inc.
FDA (openFDA food enforcement)
Reported Jun 24, 2026
Product Name: STAAR ICL Calculation Software Software Version: Version 8.00 Product Description: The STAAR ICL…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Staar Surgical AG
FDA (openFDA device enforcement)
Reported Jun 24, 2026
Brand Name: HeartMate Product Name: HeartMate 3 Left Ventricular System (LVAS) Kits Model/Catalog Number: 106524US…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Thoratec LLC
2 more products in this recall
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.