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. 2,829 recalls have been distributed to North Carolina in the last 12 months.
Showing 1321–1340 of 54,363 recalls
Recalled Item: Automated Impella Controller (AIC) labeled as the following with...
The Issue: Potential for Automated Impella Controller (AIC) purge pressure issues due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bupropion Hydrochloride Extended-Release Tablets USP (XL) Recalled by...
The Issue: Failed Tablet/Capsule Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carbamazepine Extended-Release Tablets Recalled by Amerisource Health...
The Issue: Failed Dissolution Specifications.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CONSTELLATION ULTRAVIT 10K and CONSTELLATION HYPERVIT 20K Recalled by Alcon...
The Issue: XXX
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ben's Original Ready Rice Long Grain & Wild Recalled by MARS FOODS US Due to...
The Issue: Possible presence of stones in product
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ben's Original Ready Rice Original Long Grain White Recalled by MARS FOODS...
The Issue: Possible presence of stones in product
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ben's Original Ready Rice Whole Grain Brown Recalled by MARS FOODS US Due to...
The Issue: Possible presence of stones in product
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Organic BABY bedtime drops Recalled by M.O.M Enterprises, LLC. Due to...
The Issue: Potential yeast contamination.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cetirizine Hydrochloride Tablets USP 10 mg Recalled by JB Chemicals and...
The Issue: Tablet/Capsules Imprinted with Wrong ID
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cetirizine Hydrochloride Tablets USP 10 mg Recalled by JB Chemicals and...
The Issue: Tablet/Capsules Imprinted with Wrong ID
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Major ChlorproMAZINE Hydrochloride Tablets Recalled by The Harvard Drug...
The Issue: CGMP Deviations: Presence of N-Nitroso Desmethyl Chlorpromazine above the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Major ChlorproMAZINE Hydrochloride Tablets Recalled by The Harvard Drug...
The Issue: CGMP Deviations: Presence of N-Nitroso Desmethyl Chlorpromazine above the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Major ChlorproMAZINE Hydrochloride Tablets Recalled by The Harvard Drug...
The Issue: CGMP Deviations: Presence of N-Nitroso Desmethyl Chlorpromazine above the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Major ChlorproMAZINE Hydrochloride Tablets Recalled by The Harvard Drug...
The Issue: CGMP Deviations: Presence of N-Nitroso Desmethyl Chlorpromazine above the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Major ChlorproMAZINE Hydrochloride Tablets Recalled by The Harvard Drug...
The Issue: CGMP Deviations: Presence of N-Nitroso Desmethyl Chlorpromazine above the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brand Name: Galaxy System Product Name: Galaxy System Model/Catalog Number:...
The Issue: Due to Users not having access to the Instructions for Use/User Manual due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Option"ELITE Vena Cava Filter System UDI-DI code: 00886333217151 Recalled by...
The Issue: Due to complaints of increased resistance when advancing the dilator within...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiac Workstation 5000 Recalled by Philips North America Due to Failure of...
The Issue: Failure of Environmental Stress Testing from a pinched power module wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product: STA Liatest D-Di Recalled by Diagnostica Stago, Inc. Due to A...
The Issue: A potential risk of underestimation of D-Dimer (D-Di) levels with the two...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiac Workstation 7000 Recalled by Philips North America Due to Failure of...
The Issue: Failure of Environmental Stress Testing from a pinched power module wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.