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 Dec 2, 2020

AB PowerCel 230 (velvet black), REF: CI-5523-150, UDI: (01) 07630016832956 used to power the following devices: Na¿da…

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

Advanced Bionics, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 2, 2020

Titan Pump - Product Usage: indicated for male patients suffering from erectile dysfunction (impotence) who are…

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

Coloplast Manufacturing US, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Dec 2, 2020

Life2000 Ventilation System, including Life2000 Ventilator and Life2000 Compressor, Model MS-01-0118 - Product Usage:…

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

Hill-Rom Manufacturing, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 2, 2020

Box Label: ION Fully Articulating Catheter, REF 490105, VER 08 - Product Usage: used to navigate the Ion Fully…

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

Intuitive Surgical, Inc.

FDA (openFDA device enforcement)

Food

Reported Nov 25, 2020

Art Of Tea - Feel Better tea; Produced and Distributed by: Art of Tea LLC, Monterey Park, CA Directions: 1 Tbsp of tea…

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

Art Of Tea

FDA (openFDA food enforcement)

Food

Reported Nov 25, 2020

Denali Ingredients Cream Tech 250 Sour Cream Stabilizer, Item 500120-1014, 50 lb. bag. Storage: For maximum Freshness…

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

Denali Ingredients LLC

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 25, 2020

Catalog 314-13-23, Equinoxe Cage Glenoid, Posterior Augment, Left, Medium

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

Exactech, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Nov 25, 2020

John Nagle Steelhead Fillets; 1/3 lb; Iceland; N44515; Habrun ehf; Packaging date: 29 10 2020

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

John Nagle Co.

FDA (openFDA food enforcement)

Medical devices

Reported Nov 25, 2020

COAPTITE Injectable Implant, injectable, sterile, non-pyrogenic implant composed of spherical particles (75-125 microns…

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

Merz North America, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 25, 2020

Elastic Traction Device, 11mm Lower. UPN: ER56041 Reference Number: ETD-D-26-235-C-N - Product Usage: indicated for use…

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

Micro-Tech USA

FDA (openFDA device enforcement)

Food

Reported Nov 25, 2020

Trader Joe's brand Gluten Free Battered Halibut, SKU 00503822. Product of USA. Frozen product is packed in plastic bag…

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

Orca Bay Foods LLC

FDA (openFDA food enforcement)

Food

Reported Nov 25, 2020

Rosebud's brand Elderberry Syrup Kit in a 3 oz. clear stand-up pouch (GS1 Code 852782007834).

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

Rosebud's Ranch and Garden, LLC

FDA (openFDA food enforcement)

Medical devices

Reported Nov 25, 2020

Wuxi Nest, model numbers 202115, 202117, 202017, 202018 - Product Usage: Patient specimen collection.

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

Thomas Scientific

FDA (openFDA device enforcement)

Medical devices

Reported Nov 18, 2020

SUNG HWAN E&B VIVACE Shenb Innovation of Beauty Technologyt - Product Usage: intended for use in the dermatologic and…

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

Aesthetics Biomedical, Inc.

FDA (openFDA device enforcement)

Food

Reported Nov 18, 2020

Aldi Little Salad Bar Classis Coleslaw (Green cabbage and carrots), 14 oz. plastic bag UPC:0-414498-30217-7 Kroger…

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

Dole Fresh Vegetables Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Nov 18, 2020

EDI Novel Coronavirus COVID-19 IgG ELISA Kit, REF: KT-1032 Per label: This kit is intended for qualitative detection of…

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

Epitope Diagnostics, Inc.

FDA (openFDA device enforcement)

Food

Reported Nov 18, 2020

FRESH FROM MEIJER CANTALOUPE CHUNKS LARGE BOWL, 32oz Clear plastic container, UPC 219323109721. FRESH FROM MEIJER…

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

Meijer Inc./Traffic Dept.

11 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 18, 2020

OsteoBridge Intremedullary Knee Arthrodesis (IKA) nails

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

Merete Medical GmbH

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 18, 2020

QUIDEL Sofia SARS Antigen FIA IVD REF 20374

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

Quidel Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Nov 18, 2020

Niobe ES System, Models 001-006000-1 and 001-006100-1

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

Stereotaxis Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 18, 2020

XTANT Medical, ## mm x ## mm x # mm x # ,Lordotic/Packaged InTice - C, Sterile R, Single Use Only, for the following…

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

XTANT Medical

FDA (openFDA device enforcement)

Medical devices

Reported Nov 11, 2020

Aestiva/5 MRI Anesthesia System - Product Usage: The Aestiva/5 MRI Anesthesia System provides the functional feature…

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

GE Healthcare, LLC

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 4, 2020

Equinoxe Platform Fracture Stem, 6.5mm, Left - Product Usage: The Equinoxe Platform Fracture Stem is indicated for…

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

Exactech, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Nov 4, 2020

Eishindo brand "CUP JELLY (MINI); NET WT. 28.2oz (800g); 50pcs; INGREDIENTS: WATER, HIGH FRUCTOSE SYRUP, APPLE JUIC,…

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

Hadson (Toko) Trading Co., Inc.

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.