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. 1,114 recalls have been distributed to Ohio in the last 12 months.
Showing 14941–14960 of 55,415 recalls
Recalled Item: EPINEPHIrine in 0.9% Sodium Chloride Injection Recalled by SterRx, LLC Due...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fentanyl Citrate Recalled by SterRx, LLC Due to Lack of Assurance of Sterility
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NOREPINEPHRINE 4 mg per 250 mL (16 mcg per mL) in 5% Dextrose Injection...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PHENYLepherine HCL in 0.9% Sodium Chloride Recalled by SterRx, LLC Due to...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sodium Bicarbonate in 5% Dextrose Injection Recalled by SterRx, LLC Due to...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NOREPINEPHRINE Recalled by SterRx, LLC Due to Lack of Assurance of Sterility
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NOREPINEPHRINE Recalled by SterRx, LLC Due to Lack of Assurance of Sterility
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: EPINEPHIrine in 0.9% Sodium Chloride Injection Recalled by SterRx, LLC Due...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: BV Endura with Software Release 2.3- A mobile Recalled by Philips North...
The Issue: Instructions for Use do not specify the maximum surface temperature of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Azurion Interventional Fluoroscopic X-ray System with Azurion R2.2...
The Issue: (1)Start-up problem: Intermittently at start-up of the system, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Invacare AVIVA Storm RX with LiNX Gyro Power Wheelchair (with Recalled by...
The Issue: Power Wheelchairs with a LiNX Gyro component running firmware version 6.1.2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BV Pulsera with Software Release 2.3-A mobile Recalled by Philips North...
The Issue: Instructions for Use do not specify the maximum surface temperature of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Invacare AVIVA FX with LiNX Gyro Power Wheelchair (with LiNX Recalled by...
The Issue: Power Wheelchairs with a LiNX Gyro component running firmware version 6.1.2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Veradius Unity with Software Release 2.1- Amobile Recalled by Philips North...
The Issue: Instructions for Use do not specify the maximum surface temperature of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUSON Sequoia Ultrasound Imaging System with Software Version VA25A/B...
The Issue: Due to a calculation error in the measurement when using 2D trace (manual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TruDi NAV Suction Instruments: 0-Degree Recalled by Acclarent, Inc. Due to...
The Issue: Suction Instruments were incorrectly calibrated so they may not meet the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Invacare TDX SP2 with LiNX Gyro Power Wheelchair (with LiNX Recalled by...
The Issue: Power Wheelchairs with a LiNX Gyro component running firmware version 6.1.2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O3D ORCHESTRATE Orthodontic Technologies User Manual and Data Processing...
The Issue: Due to product label/labeling being altered from it's approved state.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stealthstation System w/ Stealthstation Cranial Software 3.1.1 Recalled by...
The Issue: Cranial biopsy procedure software can enter a state where the biopsy depth...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Country Time Half lemonade and Half iced tea drink mix Recalled by KRAFT...
The Issue: potential for glass and metal in product
Recommended Action: Do not consume. Return to store for a refund or discard.