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. 1,042 recalls have been distributed to North Carolina in the last 12 months.
Showing 20661–20680 of 54,363 recalls
Recalled Item: Phenytoin Oral Suspension USP Recalled by Taro Pharmaceuticals U.S.A., Inc....
The Issue: Resuspension Problems: Two lots of Phenytoin Oral Suspension USP 125mg/5mL...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Desmopressin Acetate Tablets Recalled by American Health Packaging Due to...
The Issue: GMP Deviations: Product bottle may be absent of desiccant.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Desmopressin Acetate Tablets Recalled by American Health Packaging Due to...
The Issue: GMP Deviations: Product bottle may be absent of desiccant.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amoxicillin and Clavulanate Potassium Tablets Recalled by AuroMedics Pharma...
The Issue: Presence of Foreign Substance: Customer complaint of a foreign substance...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Caduet (amlodipine besylate/atorvastatin calcium) Tablets Recalled by Pfizer...
The Issue: Defective Container: products potentially could have been packaged in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Caduet (amlodipine besylate/atorvastatin calcium) Tablets Recalled by Pfizer...
The Issue: Defective Container: products potentially could have been packaged in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: IMMULITE 2000 Systems E2 Estradiol Catalog #: US: L2KE22(D) (200 Recalled by...
The Issue: Due to high discordant Estradiol results which.potentially affects all...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 1000 Systems E2 Estradiol Catalog #: US: LKE21(D) and Recalled by...
The Issue: Due to high discordant Estradiol results which.potentially affects all...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareFusion Alaris PCA Module Recalled by CareFusion 303, Inc. Due to 1)Error...
The Issue: 1)Error 255-XX-XXX results in inability to edit settings 2)Delay options...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HEMO-10 Hemospray Endoscopic Hemostat Recalled by Wilson-Cook Medical Inc....
The Issue: Complaints that the handle and/or activation knob on Hemostat devices have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HEMO-7 Hemospray Endoscopic Hemostat Recalled by Wilson-Cook Medical Inc....
The Issue: Complaints that the handle and/or activation knob on Hemostat devices have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareFusion Alaris System Recalled by CareFusion 303, Inc. Due to 1)Error...
The Issue: 1)Error 255-XX-XXX results in inability to edit settings 2)Delay options...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VNS Therapy Programmer Recalled by LivaNova USA Inc Due to False positive...
The Issue: False positive warning may occur after: 1) VNS Generator interrogated at 0mA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareFusion Alaris Syringe Module Recalled by CareFusion 303, Inc. Due to...
The Issue: 1)Error 255-XX-XXX results in inability to edit settings 2)Delay options...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareFusion Alaris Pump Module Recalled by CareFusion 303, Inc. Due to...
The Issue: 1)Error 255-XX-XXX results in inability to edit settings 2)Delay options...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iTotal CR Knee Replacement System Recalled by Conformis, Inc. Due to A...
The Issue: A limited number of tibial trays were labeled with an incorrect serial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iTotal PS Knee Replacement System Recalled by Conformis, Inc. Due to A...
The Issue: A limited number of tibial trays were labeled with an incorrect serial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABL90 FLEX Analyzer Recalled by Radiometer Medical ApS Due to The firm...
The Issue: The firm received reports of occurrences where the barcode reader...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABL90 FLEX PLUS Analyzer Recalled by Radiometer Medical ApS Due to The firm...
The Issue: The firm received reports of occurrences where the barcode reader...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Major Extra Strength Acetaminophen Tablets Recalled by Contract Pharmacal...
The Issue: Presence of Foreign Tablets/Capsules: Complaint involving one Women's...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.