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. 1,181 recalls have been distributed to Ohio in the last 12 months.
Showing 1101–1120 of 55,415 recalls
Recalled Item: Myosa for Kids KS1 /Sp/Mb/Mp/Lb/Lc KS2 /Sc/Mb/Mc/Mp/Lb/Lc Myosa Recalled by...
The Issue: Due to firm mistakenly distributing product within the U.S. without FDA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: HeartMate Product Name: HeartMate 3 Controller (Standalone)...
The Issue: Due to potential corrosion issues associated with the Backup Battery cable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: HeartMate Product Name: HeartMate 3 Left Ventricular System...
The Issue: Due to potential corrosion issues associated with the Backup Battery cable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bk3500 Ultrasound System w/battery Recalled by B-K Medical A/S Due to GE...
The Issue: GE HealthCare has become aware that the Instructions for Use within the user...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Catalyst+ Product Name: Catalyst Recalled by C-RAD POSITIONING...
The Issue: Due to issues with the system's stereotactic radiosurgery (SRS) treatment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quantum Intersegmental Table Recalled by Pivotal Health Solutions, Inc. Due...
The Issue: The heat function may become damaged over time due to patients pressing on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: HeartMate Product Name: HeartMate II¿ Controller (standalone)...
The Issue: Due to potential corrosion issues associated with the Backup Battery cable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quantum Intersegmental Table Recalled by Pivotal Health Solutions, Inc. Due...
The Issue: The heat function may become damaged over time due to patients pressing on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Breckenridge Pharmaceutical,...
The Issue: CGMP Deviations: N-nitroso-duloxetine impurity above the safety assessment...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ketamine Hydrochloride Recalled by STAQ Pharma, Inc. Due to Labeling:...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: UUltrasound System 2300 Recalled by B-K Medical A/S Due to GE HealthCare has...
The Issue: GE HealthCare has become aware that the Instructions for Use within the user...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olopatadine Hydrochloride Ophthalmic Solution USP 0.1 % Recalled by USV...
The Issue: Failed Impurities/Degradation Specifications: The result for 'Any individual...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 1202 Flex Focus Ultrasound System Recalled by B-K Medical A/S Due to GE...
The Issue: GE HealthCare has become aware that the Instructions for Use within the user...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bk3000 Ultrasound System w/battery Recalled by B-K Medical A/S Due to GE...
The Issue: GE HealthCare has become aware that the Instructions for Use within the user...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fasenra (benralizumab) Injection Recalled by ASTRAZENECA PHARMACEUTICALS Due...
The Issue: Lack of Assurance of Sterility:
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: or BS737162 Automated Digital Cell Morphology analyzer DI-60 Recalled by...
The Issue: Automated cell-locating device barcode reader may read the barcode of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Lithotriptor Recalled by Olympus Corporation of the Americas Due...
The Issue: The device may either fail to start up, or the transducer may start briefly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mojo Max Fusion XXX Recalled by Mohamed Hagar Due to Undeclared Sildenafil
The Issue: Marketed Without an Approved NDA/ANDA-FDA analysis revealed undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carbidopa Recalled by Rising Pharma Holding, Inc. Due to Product mix up:...
The Issue: Product mix up: complaint received that sealed medication bottle contained...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Meridian Bioscience Recalled by Meridian Bioscience Inc Due to The cap on...
The Issue: The cap on the reaction buffer tube may be missing the black rubber gasket...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.