Product Recalls in Idaho
Product recalls affecting Idaho — including food, drugs, consumer products, medical devices, and vehicles distributed to Idaho. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,544 recalls have been distributed to Idaho in the last 12 months.
Showing 13861–13880 of 48,215 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: Morphine Sulfate in 0.9% Sodium Chloride Injection Recalled by SterRx, LLC...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NOREPINEPHRINE in 5% Dextrose Injection Recalled by SterRx, LLC Due to Lack...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 12 HR Allergy & Congestion Relief Fexofenadine HCl Recalled by Dr. Reddy's...
The Issue: Failed dissolution specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Antihistamine & Nasal Decongestant Recalled by Dr. Reddy's Laboratories,...
The Issue: Failed dissolution specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Antihistamine & Nasal Decongestant Recalled by Dr. Reddy's Laboratories,...
The Issue: Failed dissolution specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Allergy & Congestion Fexofenadine HCl 60 mg & Pseudoephedrine HCl Recalled...
The Issue: Failed dissolution specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fexofenadine HCl Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...
The Issue: Failed dissolution specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Allergy & Congestion Relief Allergy Relief D Recalled by Dr. Reddy's...
The Issue: Failed dissolution specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Allergy Relief D Fexofenadine HCl Recalled by Dr. Reddy's Laboratories, Inc....
The Issue: Failed dissolution specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fexofenadine HCl 60 mg/ Pseudoephedrine HCl 120 mg Extended Release Recalled...
The Issue: Failed dissolution specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Allergy Relief D Fexofenadine HCl Recalled by Dr. Reddy's Laboratories, Inc....
The Issue: Failed dissolution specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or 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: 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 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: 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: 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: 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: 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: 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.