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 Jul 10, 2019
Disposable 25GA Vitrectomy Cutter, REF NGP0025, RX Only, Abbott Medical Optics Inc., The product provides the item…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Johnson & Johnson Surgical Vision Inc.
FDA (openFDA device enforcement)
Reported Jul 10, 2019
Vereos PET/CT, Model No. 882446 Product Usage: Positron Emission Tomography (PET) and X-ray Computed Tomography (CT)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems (Cleveland) Inc.
FDA (openFDA device enforcement)
Reported Jul 10, 2019
WOODSTOCK ORGANIC GRILLED RED PEPPER, NET WT 10. OZ, packaged in a plastic packaged marked with UPC Code: 4256301714.…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.UNFI General Corporate
FDA (openFDA food enforcement)
Reported Jul 10, 2019
DVR Crosslock ePAK Screw Driver, Model Number 212000002 Product Usage: These DVR Express Disposable Instruments are…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Biomet, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 26, 2019
Advance Enforcer 35 Focal Force PTA Balloon Catheter 6mm x 4cm, 5FR/50cm, Catalog Number ASB5-35-50-6-4, REF Number…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Cook Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 26, 2019
LEEP Precision Integrated System 120V, Model LP-10-120 Product Usage: The LEEP PRECISION INTEGRATED SYSTEM l 20V…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CooperSurgical, Inc.
FDA (openFDA device enforcement)
Reported Jun 26, 2019
2.7 Degree Angled Sagittal Saw attachment (Mako Total Knee Application Only)
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 Jun 26, 2019
Cepheid Xpert C. difficile/Epi Control Panel
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Microbiologics Inc.
FDA (openFDA device enforcement)
Reported Jun 19, 2019
CardioCommand, Inc. Transesophageal Cardiac Pacing and Recording System, Model 7A, REF 0101 - Product Usage:…
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Cardiocommand Inc.
FDA (openFDA device enforcement)
Reported Jun 19, 2019
IntraClude Intra-Aortic Occlusion Device, REF: ICF100, 10.5 Fr (3.5 mm) X 39.4" (100 cm), Rx Only, Sterile EO The…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Edwards Lifesciences, LLC
FDA (openFDA device enforcement)
Reported Jun 19, 2019
Aphrodisiac Platinum 40000, Proprietary Raw Material 6000 mg, 1 count blister card, 24 cards per box, Distributed by:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Select Distributions LLC
FDA (openFDA drug enforcement)
Reported Jun 19, 2019
Terumo Advanced Perfusion System 1 Electronic Patient Gas System (EPGS), Electronic Gas Blender, Catalog #: 801188, UDI…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Terumo Cardiovascular Systems Corporation
FDA (openFDA device enforcement)
Reported Jun 12, 2019
MRSASelect, IVD, REF 63747, containing 20 plates per package. The MRSASelect is indicated for use in conjunction with…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bio-Rad Laboratories, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 12, 2019
Pericardiocentesis Catheter Set, RPN C-PCS-850, Order # G03282
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cook Inc.
3 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 12, 2019
Regimen 28 Day - Glutaraldehyde Sterilizing and Disinfecting Solution
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kerr/Pentron, dba Kerr Corporation and Pentron Clinical
FDA (openFDA device enforcement)
Reported Jun 12, 2019
Leica Cryostats, used to produce frozen sample sections for biological, medical and industrial applications, including…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Leica Microsystems, Inc.
FDA (openFDA device enforcement)
Reported Jun 12, 2019
ECMO Reinforced Dual Lumen Cannula, Sterile EO, Rx Only, REF: VV16F
High riskUsing this product could cause serious injury, illness or death — stop using it now.OriGen Biomedical, Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Jun 12, 2019
Portex Blue Line Ultra Tracheostomy Tube Inner Cannula. One cannula comes inside a package which is labeled in part,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Smiths Medical ASD Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 12, 2019
Strawberry Banana Smoothie, 3.1oz, 6 pack, UPC Code 52159-70082
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stonyfield Farm
FDA (openFDA food enforcement)
Reported Jun 12, 2019
Stryker Neurovascular, AXS Infinity LS Plus Long Sheath, Rx Only, Sterile EO, USA Customer Service 855-91 NEURO…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Neurovascular
FDA (openFDA device enforcement)
Reported Jun 9, 2019
Taylor Farms Illinois, Inc. Recalls Bacon Quiche Products due to Misbranding and Undeclared Allergens
High riskUsing this product could cause serious injury, illness or death — stop using it now.Taylor Farms Illinois, Inc.
USDA FSIS
Reported Jun 5, 2019
Abbott MitraClip XTR Clip Delivery System, UDI: 08717648226366, Part: CDS0601-XTR, Sterile EO, Rx Only
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Abbott Vascular
FDA (openFDA device enforcement)
Reported Jun 5, 2019
Horizon Cardiology Hemo
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Change Healthcare Israel Ltd.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Jun 5, 2019
Dole Classic Coleslaw (US) Shredded cabbage and carrots. 14 oz. US
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dole Fresh Vegetables
1 more product in this recall
FDA (openFDA food 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.