Product Recalls in Ohio
Product recalls affecting Ohio — including food, drugs, consumer products, medical devices, and vehicles distributed to Ohio. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,542 recalls have been distributed to Ohio in the last 12 months.
Showing 38221–38240 of 55,415 recalls
Recalled Item: Fruit Tartlets Recalled by Ouhlala Gourmet Llc Due to Undeclared Milk
The Issue: Products contain undeclared milk on finished product labeling
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Fruit Tartlets Recalled by Ouhlala Gourmet Llc Due to Undeclared Milk
The Issue: Products contain undeclared milk on finished product labeling
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: AGFA Digital Radiography X-Ray System DX-D100 DX-D100 is indicated for...
The Issue: The DX-D100 User Manual already contained information about to move a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Herga foot switch Recalled by Zimmer Biomet, Inc. Due to Complaints were...
The Issue: Complaints were received reporting the system would freeze/shut down while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeadCare II Blood Lead Test Kit Recalled by Magellan Diagnostics, Inc. Due...
The Issue: LeadCare II Test Kits controls out of range
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeaterBaum Foot & Ankle Heating Pad Recalled by Ergoactives, Llc Due to...
The Issue: Products are marketed without a cleared 510k.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CDI H/S Cuvette Recalled by Sorin Group USA, Inc. Due to The CDI System 500...
The Issue: The CDI System 500 monitor displays the "H/S DISCONNECT AT CUVETTE" error...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mobile wDR motorized portable diagnostic X-ray systems. Intended for use...
The Issue: This is related to previous 806 Notifications about uncommanded movements of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEGION(TM) HEMI STEPPED Recalled by Smith & Nephew, Inc. Due to The package...
The Issue: The package for catalog item, a LEGION Hemi Stepped Tibial Wedge, 5 MM Size...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A Picture Archiving and Communication System (PACS) intended to display...
The Issue: To inform users about the possible incorrect values for Distance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy 100 Recalled by Philips Respironics Due to Software Issue
The Issue: Software Issue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Levofloxacin Tablets USP Recalled by Amerisource Health Services Due to...
The Issue: Failed Dissolution Specifications: Unexplained low out of specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nystatin Recalled by Perrigo Company PLC Due to Labeling: label error on...
The Issue: Labeling: label error on declared strength.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Nystatin Recalled by Perrigo Company PLC Due to Labeling: label error on...
The Issue: Labeling: label error on declared strength.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cyclopentolate Hydrochloride Ophthalmic Solution USP Recalled by Bausch &...
The Issue: Labeling: Incorrect or Missing Package Insert: Package insert is missing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tropicamide Ophthalmic Solution USP Recalled by Bausch & Lomb, Inc. Due to...
The Issue: Labeling: Incorrect or Missing Package Insert: Package insert is missing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tropicamide Ophthalmic Solution USP Recalled by Bausch & Lomb, Inc. Due to...
The Issue: Labeling: Incorrect or Missing Package Insert: Package insert is missing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Licorice Coughing Liquid (guaifenesin) Recalled by Master Herbs, Inc./Li Due...
The Issue: Marketed Without An Approved NDA/ANDA: presence of undeclared morphine.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Restoris Multicompartmental Knee (MCK) System RESTORIS MCK is indicated for...
The Issue: Reports where the Mylar/Tyvek pouch for RESTORIS MCK Baseplate in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OraQuick HCV Visual Panel Intended to assist new operation Recalled by...
The Issue: OraSure Technologies, Inc. discovered the package insert included with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.