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. 1,748 recalls have been distributed to North Carolina in the last 12 months.
Showing 46741–46760 of 54,363 recalls
Recalled Item: All Natural Recalled by Smiley National Inc Due to Smiley National is...
The Issue: Smiley National is voluntarily recalling all lots of Bali Kratom 40, XL...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Enhanced Maeng Da Leaf Powder Recalled by Smiley National Inc Due to Smiley...
The Issue: Smiley National is voluntarily recalling all lots of Bali Kratom 40, XL...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Enhanced Bali Leaf Powder Recalled by Smiley National Inc Due to Smiley...
The Issue: Smiley National is voluntarily recalling all lots of Bali Kratom 40, XL...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Natural Bali Kratom 40 Recalled by Smiley National Inc Due to Smiley...
The Issue: Smiley National is voluntarily recalling all lots of Bali Kratom 40, XL...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: K-Lite Knee 2 Stays with Visco Recalled by Breg Inc Due to Breg is recalling...
The Issue: Breg is recalling the Economy Elastic Knee Sleeve Open and K-Lite Knee 2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Economy Elastic Knee Sleeve Open Recalled by Breg Inc Due to Breg is...
The Issue: Breg is recalling the Economy Elastic Knee Sleeve Open and K-Lite Knee 2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REUMOFAN PLUS Tablets Recalled by Pain Free By Nature Due to Undeclared...
The Issue: Marketed Without an Approved NDA/ANDA; Product contains undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Italian blend Salad (Romaine Lettuce and Radicchio) packaged under the...
The Issue: Canadian Food Inspection Agency tested a random sample of bagged Italian...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Medtronic MiniMed Paradigm Insulin Infusion Pumps Recalled by Medtronic...
The Issue: Medtronic is recalling the Medtronic MiniMed Paradigm Insulin Infusion Pumps...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobas c8000 Modular Analyzer Series Cobas c502 Recalled by Roche Diagnostics...
The Issue: The Initial Cassette Volume Check (ICVC) is not activated on the cobas c 502...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merit Custom Syringe Kit Recalled by Merit Medical Systems, Inc. Due to The...
The Issue: The products are labeled as sterile but were not sterilized.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pressure Monitoring Tubing Recalled by Merit Medical Systems, Inc. Due to...
The Issue: The products are labeled as sterile but were not sterilized.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perrigo Recalled by Paddock Laboratories, LLC Due to Presence of Particulate...
The Issue: Presence of Particulate Matter Perrigo is recalling seven lots of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: IntelliSpace Portal (ISP) Recalled by Philips Medical Systems (Cleveland)...
The Issue: During SPECT reconstructions using Attenuation Correction and Scatter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAPIO Recalled by Teleflex Medical Due to The product did not meet minimum...
The Issue: The product did not meet minimum and/or average minimum Teleflex resorption...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dekna-lok Recalled by Teleflex Medical Due to The product did not meet...
The Issue: The product did not meet minimum and/or average minimum Teleflex resorption...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5/10 mm Weck Vista Optical Bladeless Laparoscopic Access Port Recalled by...
The Issue: Complaints of leakage of insufflation gas through the device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10mm Weck Vista Cannula-only Recalled by Teleflex Medical Due to Complaints...
The Issue: Complaints of leakage of insufflation gas through the device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 5/10/12 mm x 100mm Weck Vista Universal Cone Open Access Recalled by...
The Issue: Complaints of leakage of insufflation gas through the device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Weck Vista Universal Laparoscopic Port Recalled by Teleflex Medical Due to...
The Issue: Complaints of leakage of insufflation gas through the device.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.