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. 1,839 recalls have been distributed to Idaho in the last 12 months.
Showing 25441–25460 of 48,215 recalls
Recalled Item: Foley Catheter with temperature sensor 400TM 18FR Recalled by Degania...
The Issue: The catheters are suspected to contain defective sensors; if used, defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Foley Temperature Sensor Catheter 10FR Recalled by Degania Silicone, Ltd....
The Issue: The catheters are suspected to contain defective sensors; if used, defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Foley Catheter with temperature sensor 400TM 12FR Recalled by Degania...
The Issue: The catheters are suspected to contain defective sensors; if used, defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania...
The Issue: The catheters are suspected to contain defective sensors; if used, defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BBL GC-Lect Agar Recalled by Becton Dickinson & Co. Due to A portion of...
The Issue: A portion of this lot was manufactured using Gentamicin instead of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percepta CRT-P MRI SureScan Recalled by Medtronic Inc., Cardiac Rhythm and...
The Issue: Potential for a device reset to occur in Percepta CRT-P MRI SureScan and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percepta Quad CRT-P MRI SureScan Recalled by Medtronic Inc., Cardiac Rhythm...
The Issue: Potential for a device reset to occur in Percepta CRT-P MRI SureScan and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percepta Quad CRT-P MRI SureScan Recalled by Medtronic Inc., Cardiac Rhythm...
The Issue: Potential for a device reset to occur in Percepta CRT-P MRI SureScan and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic EnTrust Dual Chamber Implantable Cardioverter Defibrillator with...
The Issue: Medtronic has become aware of a potential for loss of high voltage and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic EnTrust Escudo D144DRG (OUS distribution) Product Usage: The...
The Issue: Medtronic has become aware of a potential for loss of high voltage and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic EnTrust SingleChamber Implantable Cardioverter Defibrillator with...
The Issue: Medtronic has become aware of a potential for loss of high voltage and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic EnTrust Dual Chamber Implantable Cardioverter Defibrillator with...
The Issue: Medtronic has become aware of a potential for loss of high voltage and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic EnTrust SingleChamber Implantable Cardioverter Defibrillator with...
The Issue: Medtronic has become aware of a potential for loss of high voltage and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percepta CRT-P MRI SureScan Recalled by Medtronic Inc., Cardiac Rhythm and...
The Issue: Potential for a device reset to occur in Percepta CRT-P MRI SureScan and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic EnTrust Escudo D144VRC (OUS distribution) Product Usage: The...
The Issue: Medtronic has become aware of a potential for loss of high voltage and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gaia Kratom (mitragyna speciosa) powder Recalled by Gaia Ethnobotanical LLC...
The Issue: Microbal Contamination of Non-Sterile Product; FDA analysis found salmonella...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gaia Kratom (mitragyna speciosa) powder Recalled by Gaia Ethnobotanical LLC...
The Issue: Microbal Contamination of Non-Sterile Product; FDA analysis found salmonella...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gaia Kratom (mitragyna speciosa) powder Recalled by Gaia Ethnobotanical LLC...
The Issue: Microbal Contamination of Non-Sterile Product; FDA analysis found salmonella...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gaia Kratom (mitragyna speciosa) powder Recalled by Gaia Ethnobotanical LLC...
The Issue: Microbal Contamination of Non-Sterile Product; FDA analysis found salmonella...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gaia Kratom (mitragyna speciosa) powder Recalled by Gaia Ethnobotanical LLC...
The Issue: Microbal Contamination of Non-Sterile Product; FDA analysis found salmonella...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.