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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 Jan 5, 2022

Karl Storz Udel Sterilization Tray Instructions for Use, Tray Part Number/Description: 39301ACTS/CAMERA TRAY (STERRAD,…

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

Karl Storz Endoscopy

FDA (openFDA device enforcement)

Medical devices

Reported Jan 5, 2022

Atellica CH ¿2-Microglobulin (B2M) -M) Assay for in vitro diagnostic use in the quantitative determination of…

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

Siemens Healthcare Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Jan 5, 2022

ARTISTE with syngo RT Therapist-linear accelerator systems to deliver X-Ray photon and electron radiation for the…

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

Siemens Medical Solutions USA, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 29, 2021

TruDi NAV Suction Instruments: 0-Degree, REF: TDNS000Z; 70-Degree, REF: TDNS070Z; and 90-Degree, REF: TDNS090Z

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

Acclarent, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 29, 2021

SYNCHRON Systems Cholesterol (CHOL) Reagent, REF: 467825

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

Beckman Coulter Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 29, 2021

WIRION EMBOLIC PROTECTION SYSTEM, Delivery Catheter and Filter and Retrieval Catheter, 6Fr, REF (Model Number) WRN-D6

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

Cardiovascular Systems Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 29, 2021

Leica Microsystems M220 F12 Microscope Systems

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

Leica Microsystems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 29, 2021

Stanbio TDM/B-Hydroxybutyrate Tri-Level Controls, Ref. No. 2460-605

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

MEDLINE INDUSTRIES, LP - Northfield

FDA (openFDA device enforcement)

Medical devices

Reported Dec 29, 2021

Stealthstation System w/ Stealthstation Cranial Software 3.1.1,3.1.2,3.1. or SynergyCranial Software. Synergy Cranial,…

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

Medtronic Navigation, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 29, 2021

Custom Assemblies, Inc., Single Spike Tumescent Set w/o Chamber, Reorder Number CMS-1212NS Bulk

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

Stradis Medical, LLC dba Stradis Healthcare

FDA (openFDA device enforcement)

Medical devices

Reported Dec 22, 2021

Box Label: activ5 TINY GYM IN YOUR POCKET activbody Model: Activ5 User Manual: ACTIV5 USER MANUAL Welcome to Activ5,…

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

Activbody, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Dec 22, 2021

Boston Scientific ROTAPRO, Rotational Atherectomy System Console, Model numbers H74939309010 (US) and H74939309030 (EU).

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

Boston Scientific Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Dec 22, 2021

Bartels Legionella Urinary Antigen- an adjunct to culture for the presumptive diagnosis of past or current…

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

Clark Laboratories, Inc.

FDA (openFDA device enforcement)

Food

Reported Dec 22, 2021

Krispy Kreme DOUGHNUT Bites ORIGINAL GLAZED 5 1.6 OZ (45g) POUCHES NET WT. 8 OZ (227g) Manufactured under the authority…

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

Krispy Kreme Doughnut Corporatio

FDA (openFDA food enforcement)

Medical devices

Reported Dec 22, 2021

MENTOR Saline-Filled Breast Implants are constructed from room temperature vulcanized silicone elastomer, made of…

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

Mentor Texas, LP.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 22, 2021

Miami J Select Collar, Item: MJS-101, and Miami J Select Collar Set, Item: MJSR-101 Instructions for Use

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

Ossur Americas

FDA (openFDA device enforcement)

Medical devices

Reported Dec 22, 2021

smith&Nephew EVOS MEDIAL DISTAL FEMUR PLATE, L, 5H, 90MM, REF 72573101

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

Smith & Nephew, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Dec 22, 2021

The Mustard Man Inc Simply Peppered Mustard 8oz plastic bottles, 6 bottles per case

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

The Mustard Man Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 15, 2021

SuperCore Biopsy Instrument: REF/Product Description: 701114090/SUPERCORE BIOPSY INSTR 14GA X 9CM; 701114150/SUPERCORE…

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

Argon Medical Devices, Inc.

FDA (openFDA device enforcement)

Food

Reported Dec 15, 2021

GERBER Macaroni and Cheese with a side of peas and carrots, 6.6 oz. (187 g) drained weight 5.3 oz. (150 g), 8 units per…

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

Gerber Products Company dba Nestle Infant Nutrition

FDA (openFDA food enforcement)

Food

Reported Dec 15, 2021

Mountain Meadow Herbs Brand Candida Flush Endotoxin Cleans3, 500 mg per capsule, 240 capsules per bottle. UPC 8 13086…

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

Mountain Meadow Herbs, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Dec 15, 2021

O3D ORCHESTRATE Orthodontic Technologies User Manual and Data Processing Instructions (model preparation for tooth…

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

Orchestrate Orthodontic Technologies, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Dec 15, 2021

OsteoMed OsteoPower Power Console: -OsteoMed OsteoPower Power Console 2 REF 450-0021-00 -OsteoMed D-Power Control…

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

Osteomed, LLC

FDA (openFDA device enforcement)

Food

Reported Dec 15, 2021

Trader Joe's Organic Blue Corn Tortilla Chips: 16 oz. bag, 15 bags per case

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

Trader Joes Company

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.