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. 2,801 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
2,801 in last 12 months

Showing 61016120 of 54,363 recalls

FoodMay 1, 2024· GRANDE CHEESE COMPANY

Recalled Item: Grande Bravo 250 Functional Whey Protein SKU 32101. Grade A. Recalled by...

The Issue: Possible Salmonella contamination.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodMay 1, 2024· GRANDE CHEESE COMPANY

Recalled Item: Grande Ultra 8000 Nutritional Whey Protein Isolate. SKU 32200. 80% Recalled...

The Issue: Possible Salmonella contamination.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodMay 1, 2024· GRANDE CHEESE COMPANY

Recalled Item: Grande Ultra 9100 Functional Whey Protein Isolate. SKU 32131. 90% Recalled...

The Issue: Possible Salmonella contamination.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodMay 1, 2024· GRANDE CHEESE COMPANY

Recalled Item: Grande Lactose. SKU 30601. Grade A. Pasteurized. Net Wt Recalled by GRANDE...

The Issue: Possible Salmonella contamination.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodMay 1, 2024· GRANDE CHEESE COMPANY

Recalled Item: Grande Lactose SKU 30600. Grade A. Pasteurized. Net Wt Recalled by GRANDE...

The Issue: Possible Salmonella contamination.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodMay 1, 2024· GRANDE CHEESE COMPANY

Recalled Item: Grande Grande Primo Y45 Cultured Dairy Product. Product Code: 32400....

The Issue: Possible Salmonella contamination.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodMay 1, 2024· GRANDE CHEESE COMPANY

Recalled Item: Grande Bravo 600 Functional Whey Protein SKU 32106. 34% Protein. Recalled by...

The Issue: Possible Salmonella contamination.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodMay 1, 2024· GRANDE CHEESE COMPANY

Recalled Item: Grande Bravo 500 Functional Whey Protein SKU 32103. 34% Protein. Recalled by...

The Issue: Possible Salmonella contamination.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodMay 1, 2024· GRANDE CHEESE COMPANY

Recalled Item: Grande Ultra 9150 Whey Protein Isolate. Product Code: 32324. 90% Recalled by...

The Issue: Possible Salmonella contamination.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
DrugMay 1, 2024· Dr. Reddy's Laboratories, Inc.

Recalled Item: Sirolimus Tablets 1mg Tablets 100-count bottle Recalled by Dr. Reddy's...

The Issue: Failed Impurities/Degradation Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugMay 1, 2024· Pharma Nobis LLC

Recalled Item: Meijer Magnesium Citrate Saline Laxative Oral Solution Dye Free Recalled by...

The Issue: Microbial Contamination of Non-Sterile Products - Presence of Acetobacter...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugMay 1, 2024· Pharma Nobis LLC

Recalled Item: CVS Health Magnesium Citrate Saline Laxative Oral Solution DYE FREE Recalled...

The Issue: Microbial Contamination of Non-Sterile Products - Presence of Acetobacter...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 1, 2024· Mermaid Medical A/S

Recalled Item: The D*Clot¿ HD Rotational Thrombectomy System is a percutaneous...

The Issue: Internal product testing failed bubble leak testing (ASTM F2096), which...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugApril 30, 2024· Viatris Inc

Recalled Item: Cardura XL (doxazosin) extended release tablets 8mg Recalled by Viatris Inc...

The Issue: Failed Impurities/Degradation Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 30, 2024· Viatris Inc

Recalled Item: Cardura XL (doxazosin) extended release tablets 4mg Recalled by Viatris Inc...

The Issue: Failed Impurities/Degradation Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugApril 30, 2024· Hikma Injectables USA Inc

Recalled Item: Fentanyl 1000mcg/100mL (10mcg/mL) in 0.9% Sodium Chloride Injection Recalled...

The Issue: Labeling: Wrong Barcode

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceApril 30, 2024· ZOLL Medical Corporation

Recalled Item: ZOLL 731 Ventilator (EMV+ Recalled by ZOLL Medical Corporation Due to...

The Issue: Operator's Guide & Quick Guide (QRG) ZOLL 731 Ventilator for MRI Compatible...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceApril 30, 2024· Outset Medical, Inc.

Recalled Item: TabloCart with Prefiltration Drawer PN-0006813 Recalled by Outset Medical,...

The Issue: A cart with prefiltration drawer, an optional hemodialysis system accessory,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 30, 2024· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE STERILE IRIS SCISSORS CVD/STD (case) and DYNJ04049H Recalled by...

The Issue: There is the potential of the tip protector to fall off 4.5" sterile,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugApril 29, 2024· Breckenridge Pharmaceutical, Inc

Recalled Item: Duloxetine Delayed-Release Capsules Recalled by Breckenridge Pharmaceutical,...

The Issue: CGMP Deviations: Presence of N-nitroso-duloxetine impurity above FDA...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund