Product Recalls in South Carolina
Product recalls affecting South Carolina — including food, drugs, consumer products, medical devices, and vehicles distributed to South Carolina. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,672 recalls have been distributed to South Carolina in the last 12 months.
Showing 12381–12400 of 28,688 recalls
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: 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.
Recalled Item: Medtronic Simulus 750 Flexible Ring/Band Accessory Kit - Product Usage:...
The Issue: Demonstration Simulus Reusable Sizer Accessory Kits were being incorrectly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: i-STAT G3+ cartridge (blue) Recalled by Abbott Point Of Care Inc. Due to...
The Issue: Marketed without a 510(k). Abbott Point of Care has determined that it does...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips DigiTrak XT Holter Recorder Software version number B.1 and Recalled...
The Issue: if an AAA battery is inserted in the recorder and a user attempts to start...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.