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.

Medical devices

Reported Aug 29, 2018

GE Healthcare Revolution EVO, Optima CT660, Optima CT670, Optima CT680. The systems are intended for head, whole body,…

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

GE Healthcare Japan Corporation

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Aug 29, 2018

SPARKLING GRAPEFRUIT JUICE DRINK, 6/34 oz., glass bottles

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

Gourmet International Inc.

5 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Aug 29, 2018

Graeter's HANDCRAFTED French Pot ICE CREAM, Limited Edition KEY LIME PIE**ONE PINT (473 ml)**Nutrition Facts**GLUTEN…

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

Graeters Manufacturing Company

FDA (openFDA food enforcement)

Medical devices

Reported Aug 29, 2018

Handicare C Series Patient Lift Product Usage: A device used to lift and transport a patient from one place to another.

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

Handicare USA Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 29, 2018

Johnson and Johnson Vision Care 1-Day ACUVUE MOIST Daily Wear, 8.5 Base Curve, -3.25 Power. Master Lot, containing 12…

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

Johnson & Johnson Vision Care, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 29, 2018

Liebel-Flarsheim Hydra Vision Urology X-Ray System (DR) Liebel-Flarsheim urology systems facilitate radiologic and/or…

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

Liebel-Flarsheim Company LLC

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Aug 29, 2018

Chocolate Gooey Brownie Ice Cream, packaged in pint-sized containers (473 mL), net wt 378 g; 1 gal. container, or 3…

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

Salt & Straw LLC

FDA (openFDA food enforcement)

Meat & poultry

Reported Aug 29, 2018

Taylor Farms Illinois, Inc. Retira Productos De Pastel De Carne Y Cerdo Debido A Errores De Rotulacin Y Alrgenos No…

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

Taylor Farms Illinois, Inc.

USDA FSIS

Food

Reported Aug 29, 2018

Boar's Head Brand Sweet Vidalia Onions in Sauce, glass jars 9oz UPC 0 42421 06956 3 & 64 oz UPC 0 42421 26517 0.…

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

Vidalia Valley, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Aug 29, 2018

The Tri-Flo Subglottic Suction System

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

Vyaire Medical

FDA (openFDA device enforcement)

Medical devices

Reported Aug 29, 2018

Connecting Bolt, Model 14-442093

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

Zimmer Biomet, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 22, 2018

HANDS-OFF Multi-Lumen Central Venous Catheter with Blue FlexTip for use only with Arrow One-Piece Percutaneous Sheath…

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

Arrow International Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 22, 2018

20 cm (8") PUR Smallbore Ext Set w/3-Port NanoClave Manifold, Check Valve, NanoClave, Rotating Luer single use,…

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

ICU Medical de Mexico, S.A. de C.V.

19 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 22, 2018

Rio System Irrigation Clip - Catalog # 111690 Product Usage: The RESTORIS Partial Knee Application (PKA) for use with…

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

Mako Surgical Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Aug 22, 2018

1mL Medallion Syringes Are used to inject fluids into, or withdraw fluids from the body.

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

Merit Medical Systems, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 22, 2018

MEVION S250/MEVION S250i Proton Beam Radiation therapy system Product Usage: Indicated for the delivery of radiation…

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

Mevion Medical Systems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 22, 2018

CDI Blood parameter monitoring system 500 H/SAT, Part No. 145883 Product Usage: The CDI System 500 provides continuous,…

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

Terumo Cardiovascular Systems Corporation

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Aug 15, 2018

AnnaSea Wasabi Ahi Poke Hawaiian Poke Kits

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

Aldi Inc.

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 15, 2018

Slit Knife 2.6mm 45degree Bevel Up, Model Number 373726. for use in ophthalmic surgery.

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

Beaver Visitec

FDA (openFDA device enforcement)

Medical devices

Reported Aug 15, 2018

Boston Scientific Guider Softip XF Guide Catheter Product Usage: Is a neurovascular access catheter that creates a…

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

Boston Scientific Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Aug 15, 2018

119" Blood Set w/200 Micron Filter, Clave¿, Rotating Luer, Sterile The blood tubing accessory with CLAVE Connector is a…

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

ICU Medical, Inc.

52 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 15, 2018

Leica M530 OHX Microscope System Supplied with 100 - 120 Vac.

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

Leica Microsystems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 15, 2018

Natus Neurology ErgoJust Carts labeled as the following: ICU Cart Export For PTZ Video Ext, IP PTZ HD ErgoJust Video…

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 15, 2018

Medfusion Syringe Infusion Pump, containing the Barrel Clamp Guide mechanism

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

Smiths Medical ASD 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.