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 May 20, 2026
Frederik's by meijer Vanilla Bourbon Trail Mix, packed in plastic retail-sized black bag NET WT 9 OZ (255g). On the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ferris Coffee and Nut Company, Inc.
FDA (openFDA food enforcement)
Reported May 20, 2026
LUCAS 2 Model Number: 99576 Catalog Numbers: 99576-000024 and 99576-000011 UDI-DI code: 00883873904565 LUCAS 3 Model…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Jolife AB
FDA (openFDA device enforcement)
Reported May 13, 2026
ERBEFLO CleverCap CO2: Hybrid CO2 Tubing/Cap Set for Olympus Scopes & CO2 Sources, REF: 20325-239; Hybrid CO2…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Erbe Medical, LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported May 13, 2026
french broad CHOCOLATE bette's bake sale (a multi-flavor bonbon assortment). 6-piece NET WT. 2.5 OZ (70.75G); 12-piece…
High riskUsing this product could cause serious injury, illness or death — stop using it now.French Broad Chocolate Factory
FDA (openFDA food enforcement)
Reported May 13, 2026
Intuitive 8 mm SureForm 30 Gray Reloads Reference Numbers: 48230M-05 and 48230M-06
High riskUsing this product could cause serious injury, illness or death — stop using it now.Intuitive Surgical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 13, 2026
LIFEPAK 15, REF: 99577-000025, 99577-000047, 99577-001256, 99577-001217, 99577-001241, 99577-001255, 99577-001219,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Physio-Control, Inc.
FDA (openFDA device enforcement)
Reported May 13, 2026
Brand Name: Spacelabs Ultraview SL Command Module Product Name: SL Command Module Model/Catalog Number: 91496 Software…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Spacelabs Healthcare, Inc.
FDA (openFDA device enforcement)
Reported May 13, 2026
VOCSN V+Pro package, REF: PRT-01198-000; VOCSN V+Pro unit, REF: PRT-01185-000
High riskUsing this product could cause serious injury, illness or death — stop using it now.Ventec Life Systems, Inc.
FDA (openFDA device enforcement)
Reported May 6, 2026
Brand Name: HiResolution" Bionic Ear System Product Name: M Zn-Air Battery Pak Model/Catalog Number: CI-5501-110;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Advanced Bionics, LLC
FDA (openFDA device enforcement)
Reported May 6, 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 May 6, 2026
Brand Name: Kiwi Omni Vacuum Delivery System Product Name: Kiwi Omni Vacuum Delivery System Model/Catalog Number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Clinical Innovations, LLC
FDA (openFDA device enforcement)
Reported May 6, 2026
Brand Name: Leksell Vantage Arc System REF: 1053958
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
FDA (openFDA device enforcement)
Reported May 6, 2026
Negita Cracker- Shrimp 2.8oz
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hadson (Toko) Trading Co. Inc.
FDA (openFDA food enforcement)
Reported May 6, 2026
Straumann n!ce PMMA Full-arch Restoration. Screw-retained Bridge. Article 010.0304. Endosseous Dental Implant Abutments
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Straumann USA LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 6, 2026
Brand Name: Disposable Mixing Bowls with Spatula Product Name: Mixing Bowl and Spatula Model/Catalog Number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer, Inc.
FDA (openFDA device enforcement)
Reported Apr 29, 2026
Diversatek Healthcare Viper¿ 3-Stage Fixed Wire Balloon Dilator, 6mm-7mm-8mm, REF 1204-08
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Diversatek Healthcare
3 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 29, 2026
Bulk Horchata Powder 3951 (100547) 1/25 HORCHATA UPC: 042743-19015-0 Item: 100547
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Marquez Brothers International, Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 29, 2026
CHIPS AHOY! Baked Bites Brookie .22.4 oz Carton ( 2.8 oz pouch ) and 7.7 oz Carton ( 1.4 oz pouch)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mondelez Global LLC
FDA (openFDA food enforcement)
Reported Apr 29, 2026
Oxoid Agglutinating Sera, Salmonella 9-0 R30957301
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Remel Europe Ltd.
FDA (openFDA device enforcement)
Reported Apr 29, 2026
Flamingo Funnel Small, Model Number SQ20012-01
Moderate riskThis product could cause temporary or reversible health problems — stop using it.SurgiSmoke Solutions
2 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 22, 2026
iLet Ace Pump Kit REF: BB1001 iLet Dosing Decision Software
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beta Bionics, Inc.
FDA (openFDA device enforcement)
Reported Apr 22, 2026
Gentuity HF-OCT Imaging System Model G10-01; Software version 23.2.13;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Gentuity, LLC
FDA (openFDA device enforcement)
Reported Apr 22, 2026
Cytal Wound Matrix 2-Layer 5x5 cm. Product ID: WSM0505.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp. (NeuroSciences)
4 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 22, 2026
Instinct Plus Endoscopic Clipping Device REF: G58010 Rx Only, Sterile EO
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Wilson-Cook Medical 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.