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. 1,003 recalls have been distributed to North Carolina in the last 12 months.
Showing 34201–34220 of 54,363 recalls
Recalled Item: 4C Homestyle All Natural Parmesan Grated Cheese Recalled by 4 C Foods, Corp....
The Issue: FDA sample revealed the presence of Salmonella contamination
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 4C All Natural Parmesan Grated Cheese Recalled by 4 C Foods, Corp. Due to...
The Issue: FDA sample revealed the presence of Salmonella contamination
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 4C All Natural 100% Imported Italian Pecorino Romano Cheese Recalled by 4 C...
The Issue: FDA sample revealed the presence of Salmonella contamination
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 4C All Natural Parmesan/Romano Grated Cheese Recalled by 4 C Foods, Corp....
The Issue: FDA sample revealed the presence of Salmonella contamination
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 4C Homestyle All Natural 100% Imported Italian Pecorino Romano Cheese...
The Issue: FDA sample revealed the presence of Salmonella contamination
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 4C Homestyle All Natural Parmesan/Romano Grated Cheese Recalled by 4 C...
The Issue: FDA sample revealed the presence of Salmonella contamination
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ImplantDirect Legacy 4 Implant Recalled by Implant Direct Sybron...
The Issue: The vial cap was mislabeled with the incorrect part number of 855708 but the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Desoximetasone Ointment USP Recalled by Akorn Inc Due to Failed Stability...
The Issue: Failed Stability Specifications; out-of specification value for homogeneity...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ultimate Body Tox PRO capsules Recalled by Ultimate Body Tox Due to...
The Issue: Marketed Without An Approved NDA/ANDA: The product contains undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brilliance 64 728231 Computed Tomography X-ray systems intended to produce...
The Issue: Software error due to the filament on timer
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core 728321 Computed Tomography X-ray systems intended to produce...
The Issue: Software error due to the filament on timer
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity CT 728326 Computed Tomography X-ray systems intended to produce...
The Issue: Software error due to the filament on timer
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core 128 728323 Recalled by Philips Medical Systems (Cleveland)...
The Issue: Software error due to the filament on timer
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 64 728232 Computed Tomography X-ray systems intended to produce...
The Issue: Software error due to the filament on timer
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Weight Watchers Smart Ones Recalled by KRAFT HEINZ FOODS COMPANY Due to...
The Issue: Possible contamination of product with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Smith & Nephew Recalled by Smith & Nephew, Inc. Due to Lack of 510k...
The Issue: Lack of 510k clearance for design modification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew Recalled by Smith & Nephew, Inc. Due to Lack of 510k...
The Issue: Lack of 510k clearance for design modification.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reprocessed Xcel Bladeless Trocar (H12LP) Model # H12LP Reprocessed...
The Issue: An increase in reports indicating that the reprocessed H12LP Trocar...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ev3 Recalled by Medtronic Inc Due to Medtronic identified an issue with...
The Issue: Medtronic identified an issue with specific models and lots of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Virtual XD Light Body Fast Set Wash Material Recalled by Ivoclar Vivadent,...
The Issue: The firm received complaints claiming the dental material failed to set up....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.