All recall categories

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 48,100 notices were distributed nationwide, so they reach Ohio too — those are in the archive.

Medical devices

Reported Sep 20, 2023

Proclaim XR 5 Implantable Pulse Genterator REF 3660 (previously known as Proclaim" 5 Elite IPG) Model 3660 Product…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Abbott Medical

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 20, 2023

FILMARRAY Gastrointestinal (GI) Panel (Part No.: RFIT-ASY-0104 & RFIT-ASY-0116) Pouch Module Software

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

BioFire Diagnostics, LLC

FDA (openFDA device enforcement)

Food

Reported Sep 20, 2023

Cassano's The Pizza King Premium Pizza Dough on Parchment: packaged as 16in (regular)

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Cassanos Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Food

Reported Sep 20, 2023

Zespri Organic Green Kiwi, product of New Zealand, perishable, packaged in plastic clamshell, net wt. 1lb. UPC…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

David Oppenheimer & Company I LLC

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Sep 20, 2023

Magnifuse Bone Graft, Large, Size: 14mm x 25mm, REF 7509014, Human Tissue, Demineralized Bone Matrix, sterile.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medtronic Sofamor Danek USA Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 20, 2023

ACUSON Redwood 2.0 ultrasound systems, REF: 11503314

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Siemens Medical Solutions USA, Inc.

FDA (openFDA device enforcement)

Meat & poultry

Reported Sep 15, 2023

American Foods Group, LLC Recalls Ground Beef Products Due to Possible E. Coli O103 Contamination

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Green Bay Dressed Beef, LLC

USDA FSIS

Food

Reported Sep 13, 2023

Nestle Toll House, Chocolate Chip Cookie Dough, 16.5 oz. Cookie dough in bar form packaged in paperboard tray with…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Nestle-USA, Inc. (Corporate Office)

FDA (openFDA food enforcement)

Medical devices

Reported Sep 13, 2023

ISee Ortho-K Lens

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

PARAGON VISION SCIENCES, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 13, 2023

Parent's Choice brand Sensitivity Premium Infant Formula, 638g, packaged in plastic tubs; and Tippy Toes brand…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

PBM Nutritionals, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Sep 13, 2023

3D9-3v Transducer, accessory to Philips Ultrasound Systems: EPIQ Elite; Affiniti 30, 50, and 70; ClearVue 850; HD15;…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips Ultrasound, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 6, 2023

LIF AMP, Adjustable Awl, REF 117-165, Part of the AMP System. Used with Spine Lateral Interbody Systems, IdentiTi LIF,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Alphatec Spine, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 6, 2023

Beckman Coulter, IVD, REF: OSR61171, IgA, 4 x 14 mL R1, 4 x 11 mL R2

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Beckman Coulter Inc.

FDA (openFDA device enforcement)

Food

Reported Sep 6, 2023

Lyons Grape Juice packaged in 4 fl oz opaque white plastic cup 96 cups per case

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Lyons Magnus LLC

2 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Sep 6, 2023

Oculus Pentacam AXL Wave, Ref 70020, CE 0123

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Oculus Optikgeraete GmbH

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 6, 2023

epoc BGEM BUN Test Card with epoc Host SW v3.37.3, epoc NXS SW v4.10.6, Sensor Configuration 41.1

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Siemens Healthcare Diagnostics Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 30, 2023

BioFire Respiratory Panel 2.1 (RP2.1), REF: 423742, For FILMARRAY systems, IVD, Rx Only

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

BioFire Diagnostics, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 30, 2023

The O-arm O2 Imaging System is a mobile x-ray system designed for 2D fluoroscopic and 3D imaging for adult and…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medtronic Navigation, Inc.-Littleton

FDA (openFDA device enforcement)

Medical devices

Reported Aug 30, 2023

Randox Liquid Urine Control Level 2- intended for in vitro diagnostic use, in the quality control of Amylase, Calcium,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Randox Laboratories Ltd.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Aug 30, 2023

Soft Serve on the Go brand Vanilla Chocolate flavor; 8 fl oz; UPC 0-91404-15129-0 Soft Serve on the Go brand Parve…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Real Kosher Ice Cream, Inc.

4 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 30, 2023

ADVIA Chemistry Urinary/Cerebrospinal Fluid Protein (UCFP), Material Number 11319151, in vitro diagnostic use in the…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Siemens Healthcare Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 23, 2023

FreeStyle Libre 2 Readers, REF: 71951-01 and 71953-01, used with FreeStyle Libre 2 System

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Abbott Diabetes Care, Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 23, 2023

Heinen's Fresh Ground Cashew Butter: packaged in plastic circle containers 1lb. Sold individually.

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Heinens

FDA (openFDA food enforcement)

Food

Reported Aug 23, 2023

IO Inspired Organics brand Organic Raw Walnut Halves & Pieces; 7oz plastic tubs; 9 packages per wholesale case; retail…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Lipari Foods Operating Company, LLC.

FDA (openFDA food enforcement)

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Other states

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.