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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 48,122 notices were distributed nationwide, so they reach Ohio too — those are in the archive.

Food

Reported Nov 27, 2019

Dry dates packaged under the following brands: Keshav Dry Yellow Dates, 7oz., UPC: 643864233124 and 14oz., UPC:…

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

Peekay International, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Nov 27, 2019

SOMATOM go.Top, Models 11061640 & 11061648- a Computer tomography x-ray system

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 Nov 21, 2019

Missa Bay, LLC Recalls Salad Products Due to Possible E. coli O157:H7 Contamination

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

Missa Bay LLC

USDA FSIS

Medical devices

Reported Nov 20, 2019

Cadence Science Pressure Control Glass Syringe, Part Nos. 5338 (GTIN #816329023381); 5339 (GTIN #816329023398); 5340…

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

Cadence Science, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 20, 2019

2.4mm x 2.5 Fluted Pin Pouch; Catalog Number: 351-90-22; Orthopedic surgical instrument used in the implantation of the…

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

Exactech, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 20, 2019

Visual-ICE Cryoablation System, FPRCH6000. The cryoablation system is a mobile console system intended for cryoablative…

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

Galil Medical, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 20, 2019

2000 Vascular with 30 Degree option

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

Heritage Medical Products, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 20, 2019

Implant Direct, REF654311U, simply InterActive Implant, Surface: SBM, Qty 1, 4.3mmD x 11.5mmL, 3.4mmD Platform, RX…

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

Implant Direct Sybron Manufacturing, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 20, 2019

ORTHOFIX Catalogue Number: ref 11007, drill bit diameter 4.8 MM LENGTH 280 MM, RX ONLY, Non Sterile, UDI:…

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

Orthofix Srl

30 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 20, 2019

ProtectIV¿ Plus Safety IV Catheter, sterile. Packaged in a pouch and than into an inner carton.

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

Smiths Medical ASD Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 13, 2019

Prismaflex Control Unit, software versions below 7.21

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

Baxter Healthcare Corporation

4 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Nov 13, 2019

Kroger Wild Caught Sockeye Salmon Boneless, Frozen, Raw, Skin-on, not ready to eat (NRTE), individually vacuum packed…

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

Cold Locker Processing LLC

FDA (openFDA food enforcement)

Food

Reported Nov 13, 2019

Sweet Smiles brand Select Dark Chocolate with Orange Peel Bar in 3.5 oz. foil wrapper packaging.

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

Dollar General Corporation

FDA (openFDA food enforcement)

Medical devices

Reported Nov 13, 2019

SPIFE Alkaline Hemoglobin Kit, Cat. No. 3415, for use in the separation and quantitation of hemoglobins by agarose…

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

Helena Laboratories, Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 13, 2019

Hitachi Scenaria Whole-body X-ray CT System

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

Hitachi Medical Systems America Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 13, 2019

StemPro¿ MSC SFM CTS"

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

Life Technologies Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Nov 13, 2019

The LivaNova VNS Therapy System, used for Vagus Nerve Stimulation (VNS), consists of an implantable VNS Therapy…

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

LivaNova USA Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Nov 13, 2019

Babi.Plus 12.5 cm H2O Pressure Relief Manifold Catalog # 2691 for use with ventilators.

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

Teleflex-Morrisville

FDA (openFDA device enforcement)

Medical devices

Reported Nov 13, 2019

Cardinal Health Brand 120mL/53mm sterile specimen container with orange cap, 75 pieces/pack, 4 packs/case Catalog…

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

Thermo Fisher Scientific (Monterrey)

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Nov 13, 2019

Season's Choice Raspberries (frozen): 12 ounce bags; Product of Chile. Item number: 076163-01 Aldi brand name Season's…

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

Wawona Frozen Foods Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Nov 13, 2019

Grab n Go Opti series VIPR system Model # PRX-9615 - Product Usage: The Grab n Go Opti system is an integrated delivery…

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

Western / Scott Fetzer Company

4 more products in this recall

FDA (openFDA device enforcement)

Meat & poultry

Reported Nov 9, 2019

Ezzo Sausage Company Retira Productos De Carne Debido A Una Posible Contaminación Con Listeria

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

Ezzo Sausage Company

USDA FSIS

Medical devices

Reported Nov 6, 2019

Various products which were contract sterilized.

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

Anewmed Corporation

FDA (openFDA device enforcement)

Drugs

Reported Nov 6, 2019

Atorvastatin Calcium Tablets, USP 40 mg*, 1,000 count bottles, Rx Only, Manufactured by: Apotex Inc. Toronto, Ontario…

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

Apotex Inc.

FDA (openFDA drug 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.