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.
5,475 stored notices name Ohio, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,759 notices were distributed nationwide, so they reach Ohio too — those are in the archive.
Reported Oct 16, 2024
Triathlon Universal TS Baseplate Size 2 - A single use sterile implantable device intended for cemented applications…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Howmedica Osteonics Corp.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 16, 2024
MEDIHONEY Dressing with Active Leptospermum Honey Wound and Burn Dressing W/APPLICATOR, 1.5oz tube (Model Number 31515)…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp.
FDA (openFDA device enforcement)
Reported Oct 16, 2024
NxTAG Respiratory Pathogen Panel, REF: I051C0447
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Luminex Molecular Diagnostics Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 16, 2024
StealthStation S8 App versions 1.3.0 and 1.3.2, (Model # 9735762) The StealthStation System, with StealthStation Spine…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Medtronic Navigation, Inc.
FDA (openFDA device enforcement)
Reported Oct 16, 2024
FastPack TSH Calibrator Kit, REF: 25000024, For use in conjunction with the FastPack IP TSH Immunoassay and FastPack IP…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Qualigen Inc.
FDA (openFDA device enforcement)
Reported Oct 16, 2024
Aligned Medical Tonsil Tray REF AMS9300A that contains the Cardinal Health Salem Sump PVC tubes. Product packaged in a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Windstone Medical Packaging, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 9, 2024
DAILIES TOTAL1, DAILIES TOTAL1 for Astigmatism, DAILIES TOTAL1 Multifocal, TOTAL30 Sphere,
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Alcon Research LLC
FDA (openFDA device enforcement)
Reported Oct 9, 2024
Whole cantaloupe, brand name Kandy, packed in a corrugated box, 9 count
High riskUsing this product could cause serious injury, illness or death — stop using it now.Eagle Produce LLC, dba Martori Farms
FDA (openFDA food enforcement)
Reported Oct 9, 2024
Sqwincher Electrolyte Beverage Mix, Orange powder pack, Net Wt 47.66 oz (3lb) 1.35 kg: UPC 7588008834 / 16 per case / 5…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kent Precision Foods Group, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Oct 9, 2024
MiniMed 630G Insulin Pump, REF: MMT-1515, MMT-1714, MMT-1715, MMT-1754, MMT-1755; MiniMed 700G Insulin Pump, REF:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Medtronic MiniMed, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 9, 2024
Miami J Select Collar, Catalog: MJS-101; Miami J Select Collar Set, Catalog: MJSR-101
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ossur H / F
FDA (openFDA device enforcement)
Reported Oct 9, 2024
Tablo Console, REF: PN-0003000, PN-0006000, part of the Tablo Hemodialysis System. The Tablo Hemodialysis System is…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Outset Medical, Inc.
FDA (openFDA device enforcement)
Reported Oct 9, 2024
DIVA 24 Inch Widescreen LCD Touch Display - Used with the Philips PIC iX system central monitoring system. Model:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America LLC
FDA (openFDA device enforcement)
Reported Oct 2, 2024
PACEMAKER PACK, SLCV01J; Medical convenience kit
Moderate riskThis product could cause temporary or reversible health problems — stop using it.American Contract Systems, Inc.
18 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 2, 2024
BioPince Ultra Full Core Biopsy Instrument: REF: REF: 360-1080-01, 360-1080-02, 360-1080-03, 360-1580-01, 360-1580-02,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Argon Medical Devices, Inc.
FDA (openFDA device enforcement)
Reported Oct 2, 2024
Montreal Fudge brand Chocolate Fudge with Nuts; 5.6oz
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Authentik Fudge
FDA (openFDA food enforcement)
Reported Oct 2, 2024
PT301US Airvo 3 Respiratory Support Device with software version 1.2.0 and/or 1.5.1 The Airvo 3 is intended to provide…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Fisher & Paykel Healthcare, Ltd.
FDA (openFDA device enforcement)
Reported Oct 2, 2024
Infla-650 Herbal Dietary Supplement, 700mg, packaged in pouches containing 60 capsules, Distributed by: Guru Inc., 4370…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Guru Inc.
FDA (openFDA drug enforcement)
Reported Oct 2, 2024
Karl Storz - Endoskope , REF: 27092AMA, Hopkins Telescope 6, Rx only, CE 0123
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Karl Storz Endoscopy
7 more products in this recall
FDA (openFDA device enforcement)
Reported Oct 2, 2024
Prelude Sheath Introducer 7.5F, REF: PSI-7F-11-038 Version F (PSI-7F-11-038/F)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Merit Medical Systems, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Oct 2, 2024
ACUSON Juniper 1.0, 1.5, 2.0, 2.5 Diagnostic Ultrasound Systems, REF: 11335791, with software. ACUSON Juniper Select…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
2 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 25, 2024
Alaris System PC Unit Model 8015 - a modular infusion pump and monitoring system
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
4 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 25, 2024
ViewPoint; system, imaging processing, radiological
Moderate riskThis product could cause temporary or reversible health problems — stop using it.GE Healthcare GmbH
1 more product in this recall
FDA (openFDA device enforcement)
Reported Sep 25, 2024
KODIAK PROTEIN-PACKED POWER WAFFLES BUTTERMILK & VANILLA NET WT 3.35 lb (53.6oz) 1.52kgCreated & distributed by: KODIAK…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Kodiak Cakes LLC
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.