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 Aug 13, 2025
One-piece Guedel airway, size 2, ISO 8.0, green. Model Number: 1112080.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Intersurgical Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 13, 2025
ARAL FISH; ARAL SILVER VOBLA; WHOLE DRIED, SALTED ROACH FISH EVISCERATED; FISH ROE DRIED; Ingredients: whole…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Krasnyi Oktyabr USA Inc.
FDA (openFDA food enforcement)
Reported Aug 13, 2025
1) OH MMB Human Donor Milk, 20.00 Cal/oz, 1.00 g/dl Protein, packaged in 3 oz plastic bottles 2) OH MMB Human Donor…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ohio Health Mother Milk Bank
FDA (openFDA food enforcement)
Reported Aug 6, 2025
SafeStar 90 Plus Filter. Bidirectionally breathing system filter.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Draeger, Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 6, 2025
HeartSine SAM 350P, HeartSine SAM 360P, and HeartSine SAM 450P The HeartSine samaritan¿ PAD (Public Access…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.HeartSine Technologies Ltd.
FDA (openFDA device enforcement)
Reported Aug 6, 2025
The Drill Stop Kit is the version of the Mini Sterilizable Tray that is used to store, sterilize, verify Drill Stop…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Implant Direct Sybron Manufacturing LLC
FDA (openFDA device enforcement)
Reported Aug 6, 2025
IontoPatch STAT, On-the-Go Patch Therapy, Model/Catalog Number D-0062-080; IontoPatch is an Iontophoresis transdermal…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LTS Therapy Systems, LLC
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 6, 2025
Phasor Drill, REF: 2.70S, 3.20L, 4.50, 5.30, 6.35
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Phasor Health, LLC
FDA (openFDA device enforcement)
Reported Aug 6, 2025
Sheehan Brothers Vending Cheeseburger, 4.7 oz (132g), individually wrapped in plastic, UPC: 100000952375
High riskUsing this product could cause serious injury, illness or death — stop using it now.Sheehan Brothers Vending
5 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 6, 2025
Volcano Visions Digital IVUS Catheter: PV.014P (Platinum), REF:85910P; PV.014P RX, REF: 014R; and PV.018, REF: 86700,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Volcano Corp.
FDA (openFDA device enforcement)
Reported Jul 30, 2025
Bridge to Life EasiSlush, (Sodium Chloride Solution for Sterile Slush Preparation) (0.9% Sodium Chloride Irrigation,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bridge to Life Ltd.
FDA (openFDA device enforcement)
Reported Jul 30, 2025
HSG Procedure Tray. Model Number: 6050T. The HSG Procedure Tray is for use in hysterosalpingography and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CooperSurgical, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jul 30, 2025
Covidien Nellcor Bedside SpO2 Patient Monitoring System: REF: PM100N, 10005941, DLPM100N, DL10005941, DSPM100N,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien
FDA (openFDA device enforcement)
Reported Jul 30, 2025
ACUVUE¿ OASYS MAX 1-Day MULTIFOCAL
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Johnson & Johnson Vision Care, Inc.
FDA (openFDA device enforcement)
Reported Jul 30, 2025
Artisan Style 1/2 Loaf, Net wt. 12 oz (340g) 024126018152 1/2 Loaf of white bread with white flour topping and two…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lewis Bakeries
FDA (openFDA food enforcement)
Reported Jul 30, 2025
PROLIA (denosumab), injection, 60mg/mL, For Subcutaneous Use Only, Rx Only, Manufactured by: Amgen Inc., Thousand Oaks,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mckesson Medical-Surgical Inc. Corporate Office
2 more products in this recall
FDA (openFDA drug enforcement)
Reported Jul 30, 2025
Sushi Wasabi; 5 grams (Ready to eat) Ingredients: Horseradish, Corn Oil, Salt, Water, Citric Acid, Tumeric, FD&C Blue#1…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ming Hong International Inc.
FDA (openFDA food enforcement)
Reported Jul 30, 2025
Ritz Peanut Butter Cracker Sandwiches, Net Wt.27.6 oz, 20 count (20x1.38 oz) 6- pack of cracker sandwiches inside…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mondelez Global LLC
3 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 30, 2025
Azurion 7 M20. Fluoroscopic X-Ray System.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems Nederland B.v.
FDA (openFDA device enforcement)
Reported Jul 30, 2025
Stryker, StrykeFlow , REF: 0250070500, 2, Disposable Suction/Irrigator without Disposable Tip
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 30, 2025
Turkeyfoot Creek Creamery Avalanche Artisan Ice Cream, One Pint (473 ml), packaged individually in a paper carton with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Turkeyfoot Creek Creamery LLC
7 more products in this recall
FDA (openFDA food enforcement)
Reported Jul 23, 2025
Baxter SIGMA Spectrum Infusion Pump V6, Model Number 35700BAX
High riskUsing this product could cause serious injury, illness or death — stop using it now.Baxter Healthcare Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jul 23, 2025
SwabCap Disinfecting Cap for Needlefree Connectors: SwabSleeve, REF: SCXT3-5-2000; SwabCap, 200-ct. Box, REF: SCXT3-2000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
FDA (openFDA device enforcement)
Reported Jul 23, 2025
i-view video laryngoscope. Model Number: 8008000. The i-view video laryngoscope is indicated to facilitate laryngoscopy.
High riskUsing this product could cause serious injury, illness or death — stop using it now.Intersurgical 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.