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

Food

Reported Aug 15, 2018

Ocean Delight Individually Vacuum Packed AHI TUNA SAKU, 8-12 oz. NET WT. 10 LB (4.54 kg) and 12-16 oz. NET WT. 22LB…

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

Stavis Seafoods, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 15, 2018

Think Surgical Cutter, Flat, ¿6.2mm x 144mm. For use only with the TCAT Computer-Assisted Tool. Part Number 106428 The…

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

Think Surgical, Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 15, 2018

utz Carolina Style Barbeque Potato Chips, Net Wt 2.875 OZ, UTZ Quality Foods, LLV, Hanover, PA 17301, UPC:…

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

Utz Quality Food Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 15, 2018

AirLife Resuscitation Device, Adult labeled as the following: a. Adult, with mask, oxygen reservoir bag, Part Number…

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

Vyaire Medical

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 15, 2018

Waterpik Sonic-Fusion Professional, Model: SF-02 Product Usage: The device is composed of a unit base and an oral…

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

Water Pik, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 8, 2018

MicroScan Pos Combo Panel Type 43, Catalog number B1017-217for use in determining antimicrobial agent susceptibility…

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

Beckman Coulter Inc.

FDA (openFDA device enforcement)

Food

Reported Aug 8, 2018

PINK LEMONADE COOKIES Byrd's FAMOUS COOKIES; NET WT. 7 OZ .(198g) BOX; BYRD COOKIE COMPANY 6700 WATERS SAVANNAH, GA…

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

Byrd Cookie Co.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 8, 2018

Drill (Fluted-Hard Bone), for Quattro Link 2.9mm, labeled as: a. Quattro Spade Drill, for 2.9mm, Model Number CM-9300;…

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

Cayenne Medical Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 8, 2018

Diamedix Is-Mumps IgG Enzyme Immunoassay Test Kit for In Vitro Diagnostic Use Catalog No. 720-540

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

Diamedix Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 8, 2018

Instrument trays used to store AltiVate Small Shell Trials (FA S ALTIVATE RSP HUM TRLS SM). Metal container with lid…

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

Encore Medical, LP

FDA (openFDA device enforcement)

Food

Reported Aug 8, 2018

Ruffles Original potato chips 9 oz. bags

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

Frito-Lay, Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 8, 2018

1) ELITE HV, Hemostasis Valve Introducer System, Sterile EO, Rx Only, Catalog #: a) BCL-100-04; b) BCL-100-05; c)…

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

Galt Medical Corporation

7 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 8, 2018

Discovery IQ 2.0 20cm, 4 ring, Model Number 5432539-22

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

GE Healthcare, LLC

9 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Aug 8, 2018

Natural Flavor Turkey Type, 40 pounds, Powder in a blue poly-lined cardboard box, Ambient

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

Innova Flavours

3 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 8, 2018

MAYFIELD INFINITY XR2 BASE UNIT, Part Number A2079 The MAYFIELD¿ Infinity XR2 Base Unit is intended to be used to…

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

Integra LifeSciences Corp.

3 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 8, 2018

Merge Unity software, formerly known as DR Systems Unity PACS software. The firm name on the label is Merge Healthcare,…

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

Merge Healthcare, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 8, 2018

XLTEK EMU40EX EEG Headbox

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

Natus Neurology dba Excel Tech., Ltd. (XLTEK)

FDA (openFDA device enforcement)

Medical devices

Reported Aug 8, 2018

Zimmer Dermatone AN, Model No. 88710100

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

Zimmer Surgical Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 1, 2018

AD-TECH Medical Instrument Corporation Drill Sleeve Guides DSG-6-3-090-2.4N utilizing raw material (RM0677) from the…

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

Ad-Tech Medical Instrument Corporation

FDA (openFDA device enforcement)

Food

Reported Aug 1, 2018

AMPI Whey Powder, Sweet Type, Formula 521, Extra Grade, spray process pasteurized, packaged in 50 lbs net (22.68 kg…

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

Ampi

FDA (openFDA food enforcement)

Medical devices

Reported Aug 1, 2018

Arctic Sun Temperature Management System, Model 5000. The Arctic Sun¿ 5000 model is a non-invasive, thermal regulating…

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

Bard Medical Division

FDA (openFDA device enforcement)

Food

Reported Aug 1, 2018

Sweet Serenity Caramel Sea Salt Chocolate Chip Cookies, with caramel flavored chips; NET WT; 2 oz. UPC: 0 31535 59962 2…

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

Biscomerica, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 1, 2018

MR Surgical Suite Option Product The MR Surgical Option when integrated with the GE Signa¿ 3.0T or 1.5T magnetic…

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

GE Medical Systems, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Aug 1, 2018

Leica Microsystems products labeled as the following: Leica M320 Microscope Systems with Article Numbers 10448419,…

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

Leica Microsystems, Inc.

FDA (openFDA device 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.