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 May 17, 2017
Anthrex Bio-SwiveLock SP Vented, 5.5mm x 24.5 mm, Self-Punching
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arthrex, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported May 17, 2017
CooperSurgical lnflatoball Latex Rubber Pessary sold as an individual unit and also part of the lnflatoball Pessary…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CooperSurgical, Inc.
FDA (openFDA device enforcement)
Reported May 17, 2017
Chili Seasoning 50 lbs INGREDIENTS: Chili Pepper, Minced Onion, Wheat Flour***CONTAINS: WHEAT spicetec¿ FLAVORS &…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Givaudan Flavours Corp.
10 more products in this recall
FDA (openFDA food enforcement)
Reported May 17, 2017
Mentor Smooth Round SPECTRUM Post- Operatively Adjustable Saline Breast Implant, Product Code: 350-1490, UDI/GTIN:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mentor Texas, LP.
FDA (openFDA device enforcement)
Reported May 17, 2017
Stryker PROFESS Registration Kit. The Stryker PROFESS Registration Kit is a member of the Navigation portfolio and is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Instruments Div.
FDA (openFDA device enforcement)
Reported May 17, 2017
Vertical Pharmaceuticals OB Complete with DHA Prenatal Multivitamin, 60 softgels Rx Only, Manufactured for: Vertical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Vertical Pharmaceuticals, Inc.
FDA (openFDA food enforcement)
Reported May 10, 2017
Safeguard Flour product code 5122286 packaged in 50 lb bags
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ardent Mills LLC USA
FDA (openFDA food enforcement)
Reported May 10, 2017
Nabelsi Thyme (also known on invoices as Zatar) 450g retail (24 packages per wholesale case) 4.5kg retail (2 bags per…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Aroma Imports Inc.
FDA (openFDA food enforcement)
Reported May 10, 2017
10.0 Grams Chili Spice Blend in packets
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arro Corporation
FDA (openFDA food enforcement)
Reported May 10, 2017
The JETSTREAM is a rotational atherectomy catheter system designed for use in debulking and treating vascular disease…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Boston Scientific Corporation
FDA (openFDA device enforcement)
Reported May 10, 2017
GERMAN CHOCOLATE KB KILLER BROWNIE¿ 3x35 CT NET WT 36 LBS (16.33 kg) CONTAINS: Milk, Nuts: Pecans, Soy, Wheat UPC…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Killer Brownie Distributing LLC
3 more products in this recall
FDA (openFDA food enforcement)
Reported May 10, 2017
Shandon Rapid Chrome Kwik-Diff Kit Part Number: 9990700 Shandon Rapid Chrome Kwik-Diff Reagent #3 Part Number 9990707…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Richard-Allan Scientific Company
FDA (openFDA device enforcement)
Reported May 10, 2017
Accu-Chek Connect Diabetes Management App versions 2.0.0, 2.0.1 and 2.1.0 for iOS and Android Product Usage: This is a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diabetes Care, Inc.
FDA (openFDA device enforcement)
Reported May 3, 2017
ViperWire Advance with Flextip Peripheral Atherectomy Guide Wire, Part Number: 7-10026-01,Model Number: VPR-GW-FT14.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cardiovascular Systems Inc.
FDA (openFDA device enforcement)
Reported May 3, 2017
Colby cheese. All affected product private labeled for other companies. Brands: Guggisberg; Dutch Farms; Meijer; Amish…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Deutsch Kase Haus, LLC
12 more products in this recall
FDA (openFDA food enforcement)
Reported May 3, 2017
Amish Creamery Butter Cheese Sold under the following brand names: Amish Classic 6 lb & 15 ib and Guggisberg 15 ib…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Guggisberg Cheese Inc.
8 more products in this recall
FDA (openFDA food enforcement)
Reported May 3, 2017
HeartWare HVAD System Controller The HeartWare Ventricular Assist System (VAS is indicated for use as a…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Heartware
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 3, 2017
Season's Choice Garden Fresh Sweet Peas, Net Wt 16 oz (1lb) 454g, Keep Frozen. UPC 41498-164294.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Lakeside Foods, Inc.
FDA (openFDA food enforcement)
Reported May 3, 2017
Donepezil HCl tablets, 10mg, packaged in 10x10 blister packs per carton (100 Unit Dose) container, Rx only,…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Mckesson Packaging Services
FDA (openFDA drug enforcement)
Reported May 3, 2017
Navitrack System - OS Knee Universal, Orthopedic Stereotaxic Instrument CAS Software application intended to assist in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Orthosoft, Inc. dba Zimmer CAS
FDA (openFDA device enforcement)
Reported May 3, 2017
Blood Agar (TSA w/ 5% Sheep Blood) Plate, For In Vitro Diagnostic Use, Remel, Lenexa, KS 66215 Product Usage: Blood…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Remel Inc.
FDA (openFDA device enforcement)
Reported May 3, 2017
uNion Cervical Plate System Product Usage: The uNion Cervical Plate System is intended for anterior fixation of the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ulrich Medical USA Inc.
FDA (openFDA device enforcement)
Reported May 3, 2017
5.5mm Diameter x 500mm CoCr Straight Rod, Model number X077-0420. The product is packaged in plastic bags with one…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Xtant Medical Inc.
FDA (openFDA device enforcement)
Reported Apr 26, 2017
INFINITY Internal Hex Healing Abutment, 4.5mm Platform, 4.7mm CW-3mm CH Straight; Product Code: 20145473 Product Usage:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ace Surgical Supply Co., 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.