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 48,123 notices were distributed nationwide, so they reach Ohio too — those are in the archive.
Reported Jun 7, 2017
Amoxicillin and Clavulanate Potassium Tablets, USP, 500 mg/125 mg, in 20 count bottles, Rx Only, Manufactured in…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Sandoz Inc.
FDA (openFDA drug enforcement)
Reported Jun 7, 2017
Angio WorkStation (XIDF-AWS801) used in conjunction with your Infinix System (INFX-8000V;INFX-8000C;INFX-8000F
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Toshiba American Medical Systems Inc.
FDA (openFDA device enforcement)
Reported Jun 7, 2017
AIA-PACK TPOAb CONTROL SET
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Tosoh Bioscience, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 7, 2017
Trident Item # 421048, Multi-Grain Alaskan Cod, Frozen, RETAIL packages, Net wt. 12 oz. UPC 0 28029 21048 4 The retail…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Trident Seafoods Corp. - Island Enterprise M/V
7 more products in this recall
FDA (openFDA food enforcement)
Reported Jun 7, 2017
Chef Pierre 10 Spinach Quiche, and 6/10 Frozen Quiche, 38 oz. packed in a paper carton, keep frozen
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tyson Foods, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Jun 7, 2017
Dolphin Inflation Device, REF 0185NA. Rx only, Sterilized using Ethylene Oxide. DOLPHIN is a single-use, sterile…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vascular Solutions, Inc.
FDA (openFDA device enforcement)
Reported Jun 5, 2017
Creation Gardens Inc. Recalls Ground Beef and Beef Primal Cut Products Due to Possible E. coli O157:H7 Contamination
High riskUsing this product could cause serious injury, illness or death — stop using it now.Creation Gardens
USDA FSIS
Reported Jun 2, 2017
P&S Bakery, Inc. Recalls Pepperoni Product Due to Possible Foreign Matter Contamination
High riskUsing this product could cause serious injury, illness or death — stop using it now.P&S Bakery, Inc.
USDA FSIS
Reported May 31, 2017
CSI, Orbital Atherectomy System (OAS) Saline Infusion Pump, Rx only, Part Number: 7-10014, Model Number: SIP-3000.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardiovascular Systems Inc.
FDA (openFDA device enforcement)
Reported May 31, 2017
Opteryx Variable Rescue Screw, Part #CP2214, UDI: *+M711CP22140/$$801716012*. Packaged in heat-sealed plastic bag.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Innovasis, Inc.
FDA (openFDA device enforcement)
Reported May 31, 2017
Merge Cardio software. The firm name on the label is Merge Healthcare, Hartland, WI. Intended to be used to acquire,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merge Healthcare, Inc.
FDA (openFDA device enforcement)
Reported May 31, 2017
Dip Trio Mix Homemade Gourmet Dip Mix Net Wt. 2.9 oz. Distributed by: Phoenix Food, LLC. Canton, TX 75103…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Phoenix Food, LLC
FDA (openFDA food enforcement)
Reported May 31, 2017
ARTISAN-STYLE PIZZA DOUGH BALL distributed under the following sizes and Product Codes: (a) 12 OZ ARTISAN-STYLE PIZZA…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Rich Products Corp.
2 more products in this recall
FDA (openFDA food enforcement)
Reported May 31, 2017
Slow Roasted Ham & Swiss Breakfast Sandwich, Fully Cooked/Keep Frozen/Perishable Net Wt 5.6 oz (159 g) MANUFACTURED…
High riskUsing this product could cause serious injury, illness or death — stop using it now.SK Food Group Groveport
FDA (openFDA food enforcement)
Reported May 25, 2017
Golden Gourmet Recalls Frozen Waffle and Turkey Sausage Products Due to Possible Listeria Contamination
High riskUsing this product could cause serious injury, illness or death — stop using it now.Golden Gourmet, LLC
USDA FSIS
Reported May 24, 2017
SoftPort Easy-Load Lens Delivery System Model: EZ-28V Is used for the folding and delivering of the LI61AO, LI61AOV, or…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bausch & Lomb Surgical, Inc.
FDA (openFDA device enforcement)
Reported May 24, 2017
ETEST ETP32 (Ertapenem) Ref. 531640, 531600, blister packaging ETEST is a quantitative technique for determining the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioMerieux SA
FDA (openFDA device enforcement)
Reported May 24, 2017
GIZA Vertebral Body Replacement
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Eden Spine Europe SA
FDA (openFDA device enforcement)
Reported May 24, 2017
Arietta 70 Ultrasound System Intended for use by trained personnel (doctor, sonographer. etc.) for the diagnostic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hitachi Medical Systems America Inc.
FDA (openFDA device enforcement)
Reported May 24, 2017
Moondance desserts gluten free Chocolate Chip Cookie Bar 12 oz (340g) UPC 36211 68096 9
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Moondance Heavenly Desserts, LLC
1 more product in this recall
FDA (openFDA food enforcement)
Reported May 24, 2017
enGen (TM) Laboratory Automation Systems using all TCAutomation(TM) Software Versions with the InOut Communication…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ortho-Clinical Diagnostics
FDA (openFDA device enforcement)
Reported May 24, 2017
Wingman 35 Crossing Catheter, 65cm, Model Numbers: WGM35065US WGM35065CE WGM35090US WGM35090CE WGM35135US WGM35135CE
High riskUsing this product could cause serious injury, illness or death — stop using it now.ReFlow Medical
FDA (openFDA device enforcement)
Reported May 24, 2017
WECK Visistat 35R Disposable Skin Stapler, Ref 528135, Rx Only, Sterile EO, Visistat is indicated for the external skin…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Teleflex Medical
FDA (openFDA device enforcement)
Reported May 17, 2017
Microfil Composite Instruments are packaged in an unsealed plastic sleeve, which is then placed in a cardboard box.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Almore International 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.