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. 1,869 recalls have been distributed to Idaho in the last 12 months.
Showing 19241–19260 of 48,215 recalls
Recalled Item: FlexTip Plus Epidural Catheterization Kit Recalled by Arrow International...
The Issue: There is the potential for various failures with the LOR (loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FlexTip Plus Combined Spinal Epidural Catheterization Set Recalled by Arrow...
The Issue: There is the potential for various failures with the LOR (loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EPIDURAL CATHETERIZATION KIT Recalled by Arrow International Inc Due to...
The Issue: There is the potential for various failures with the LOR (loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FlexTip Plus Combined Spinal Epidural Catheterization Kit Recalled by Arrow...
The Issue: There is the potential for various failures with the LOR (loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EPIDURAL CATHETERIZATION KIT Recalled by Arrow International Inc Due to...
The Issue: There is the potential for various failures with the LOR (loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FlexTip Plus Epidural Catheterization Set Recalled by Arrow International...
The Issue: There is the potential for various failures with the LOR (loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EPIDURAL CATHETERIZATION KIT Recalled by Arrow International Inc Due to...
The Issue: There is the potential for various failures with the LOR (loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FlexTip Plus Combined Spinal Epidural Catheterization Kit Recalled by Arrow...
The Issue: There is the potential for various failures with the LOR (loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FlexTip Plus Epidural Catheterization Kit Recalled by Arrow International...
The Issue: There is the potential for various failures with the LOR (loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EPIDURAL CATHETERIZATION KIT Recalled by Arrow International Inc Due to...
The Issue: There is the potential for various failures with the LOR (loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FlexTip Plus Epidural Catheterization Kit Recalled by Arrow International...
The Issue: There is the potential for various failures with the LOR (loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FlexTip Plus Epidural Catheterization Kit Recalled by Arrow International...
The Issue: There is the potential for various failures with the LOR (loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EPIDURAL CATHETERIZATION KIT Recalled by Arrow International Inc Due to...
The Issue: There is the potential for various failures with the LOR (loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FlexTip Plus Epidural Catheterization Kit Recalled by Arrow International...
The Issue: There is the potential for various failures with the LOR (loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FlexTip Plus Epidural Catheterization Kit Recalled by Arrow International...
The Issue: There is the potential for various failures with the LOR (loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nystatin Oral Suspension Recalled by Pharmaceutical Associates Inc Due to...
The Issue: Subpotent: Out of specification for assay at the 12-month time point.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: methylPREDNISolone Sodium Succinate For Injection Recalled by Hikma...
The Issue: Labeling: Incorrect Instructions: Vial label incorrectly instructs...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ormco Damon Q2 Orthodontic Metal Bracket Recalled by Ormco/Sybronendo Due to...
The Issue: The bracket torque was mislabeled on the packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BodyGuard Microset For Use with the BodyGuard Infusion Pump *** Recalled by...
The Issue: The filter installed onto the tube set may have the incorrect pore size.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Simulus 850 Semi Rigid Ring/Band Accessory Kit Used to Recalled by...
The Issue: Demonstration Simulus Reusable Sizer Accessory Kits were being incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.