Product Recalls in North Carolina
Product recalls affecting North Carolina — including food, drugs, consumer products, medical devices, and vehicles distributed to North Carolina. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,986 recalls have been distributed to North Carolina in the last 12 months.
Showing 14941–14960 of 29,737 recalls
Recalled Item: PageWriter TC20 Recalled by Philips North America, LLC Due to Philips...
The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PageWriter TC30 Recalled by Philips North America, LLC Due to Philips...
The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PageWriter TC30 w/o trolley Government Bundle Recalled by Philips North...
The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PageWriter TC30 w/ trolley Government Bundle Recalled by Philips North...
The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PageWriter TC70 w/trolley Government Bundle Recalled by Philips North...
The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PageWriter TC70 w/o trolley Government Bundle Recalled by Philips North...
The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PageWriter TC50 Government Bundle Recalled by Philips North America, LLC Due...
The Issue: Philips PageWriter TC cardiograph batteries which have reached end of life...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A LINK Z INTERVERTEBRAL BODY FUSION DEVICE Product Description: A Recalled...
The Issue: Due to a manufacturing process issue, it allowed vertebral body bone screws...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A LINK Z INTERVERTEBRAL BODY FUSION DEVICE Product Description: A Recalled...
The Issue: Due to a manufacturing process issue, it allowed vertebral body bone screws...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Universa Firm Ureteral Stent Recalled by Cook Inc. Due to The wire guide may...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PTFE Wire Guide Recalled by Cook Inc. Due to The wire guide may be...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Angled Tip Ureteral Catheter Set with Bentson PTFE Wire Guide Recalled by...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bander Ureteral Diversion Open-End Stent Set Recalled by Cook Inc. Due to...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Urethral Dilation Balloon Catheter with Open Tip Recalled by Cook Inc. Due...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C-Flex Double Pigtail Ureteral Stent Set Recalled by Cook Inc. Due to The...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percutaneous Entry Set Recalled by Cook Inc. Due to The wire guide may be...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sof-Flex Double Pigtail Ureteral Stent Set Recalled by Cook Inc. Due to The...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kwart Retro-Inject Ureteral Stent Set Recalled by Cook Inc. Due to The wire...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wire Guide Recalled by Cook Inc. Due to The wire guide may be incorrectly...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Urethral Dilator Set Recalled by Cook Inc. Due to The wire guide may be...
The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.