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 Sep 13, 2018
Bob Evans Farms Inc. Retira Productos De Salchicha De Cerdo Debido A Una Posible Contaminacin Con Materia Extraa
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BEF Foods, Inc.
USDA FSIS
Reported Sep 12, 2018
Zenlens Toric-Gas Permeable Contact lenses for Daily Wear in a 10-cc polycarbonate vial (Rx) as follows: Zenlens…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Alden Optical
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 12, 2018
Overhead Counterpoise Systems (OCS), OCS CONF,STD CEIL MNT, STD HORZ ARM, Catalog # OCS 115A, Material Number 59880253
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bayer Medical Care, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 12, 2018
DRAD-3000E (Radrex-i) TFP-4336W (Wireless FPD)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Canon Medical System, USA, Inc.
FDA (openFDA device enforcement)
Reported Sep 12, 2018
Tibial Alignment Guide, REF 351-10-00 Vantage Fixed Ankle system components for ankle replacements.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Exactech, Inc.
FDA (openFDA device enforcement)
Reported Sep 12, 2018
Fresh Express Chopped Romaine 1 lb
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fresh Express Incorpated
2 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 12, 2018
VidiStar(TM) PACS & DICOM Viewer Software system
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hitachi Healthcare Americas Corp. Informatics Division
FDA (openFDA device enforcement)
Reported Sep 12, 2018
Inspire II Model 3024 Implantable Pulse Generator (IPG) for Obstructive Sleep Apnea, Inspire Part #900-003-020, Product…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Inspire Medical Systems Inc.
FDA (openFDA device enforcement)
Reported Sep 12, 2018
McKesson Cardiology Hemo, Release SW version 13.0. Used for physiological monitoring, image and data processing.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.McKesson Israel Ltd.
FDA (openFDA device enforcement)
Reported Sep 12, 2018
Baby Quasar Plus, Light Therapy System, packaging, box, sleeve and user manual. Handheld Wrinkles Reduction Device.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Quasar Bio-Tech, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 12, 2018
Virt-Nate Tablets, Number of units per package: 100 Tablets Package Type: 100 Tablets/Bottle
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Virtus Pharmaceuticals Llc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Sep 11, 2018
CTI Foods LLC Recalls Ready-To-Eat Philly Steak Products Due to Possible Listeria Contamination
High riskUsing this product could cause serious injury, illness or death — stop using it now.CTI Foods LLC.
USDA FSIS
Reported Sep 5, 2018
FLOSEAL Special Applicator Tips in cartons labeled in part, "Floseal SPECIAL APPLICATOR TIPS***6 x Malleable Tip…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Baxter Healthcare Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 5, 2018
Caito Foods, LLC Retira Productos De Ensalada De Pollo Debido A Un Error De Rotulacin Y Un Alrgeno No Declarado
High riskUsing this product could cause serious injury, illness or death — stop using it now.Caito Foods, LLC
USDA FSIS
Reported Sep 5, 2018
equate High Performance Protein Shake: Chocolate, Naturally & Artificially Flavored, ready to drink; 11 FL OZ (325 mL),…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.California Natural Products
FDA (openFDA food enforcement)
Reported Sep 5, 2018
Premo Brand Turkey & Cheese Wedge sandwiches 5 OZ retail UPC 612510002018 Plastic triangle sandwich wedge container…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lipari Foods Operating Company, LLC dba JLM Manufacturing
FDA (openFDA food enforcement)
Reported Sep 5, 2018
Stryker Mako Vizadisc Knee Procedure Tracking Kit
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mako Surgical Corporation
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 5, 2018
Medline 0.9 % Sodium Chloride Injection, USP 5 mL in 10 mL Syringe ZR Intended for flushing IV catheters and IV tubing…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medline Industries Inc.
FDA (openFDA device enforcement)
Reported Sep 5, 2018
QUIKFLAP, 3 X 2-HOLE DOG BONE PLATES WITH 1.5X4MM SELF DRILLING SCREWS, Part Number 12-01520S The Stryker QuickFlap…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Leibinger GmbH & Co. KG
17 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 29, 2018
Dymaxeon 5.5 Curved Rod Size 5.5 x 110mm (Yellow), Model Number 06.6441B Product Usage: The Dymaxeon Spine System is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Back 2 Basics Direct LLC
FDA (openFDA device enforcement)
Reported Aug 29, 2018
bioM¿rieux VITEK 2 NH ID Test Kit Product Usage: Is an automated system consisting of instruments, software and reagent…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomerieux Inc.
FDA (openFDA device enforcement)
Reported Aug 29, 2018
CAREstream ProNox Nitrous Oxide Delivery System labeled as the following: a. CMI-0100 PNX, Pro-Nox Mixer - Canadian; b.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CAREstream Medical LLC
FDA (openFDA device enforcement)
Reported Aug 29, 2018
Dole Classic Coleslaw, 14 oz. (397 g) plastic bag; Green Cabbage, shredded carrots. UPC Code 7143001066 Distributed by…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dole Fresh Vegetables Inc.
FDA (openFDA food enforcement)
Reported Aug 29, 2018
ELEKTA Digital Accelerator under the following brand names: Elekta Synergy, Synergy S, Synergy Platform, Precise…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Elekta, Inc.
1 more product 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.