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 22521–22540 of 54,363 recalls
Recalled Item: Bubbies Mochi Ice Cream -Mango Item Code CS800037 Recalled by Bubbies...
The Issue: Bubbies Mochi Ice Cream, Bubbles Cookie Dough Ice Cream Bites,Trader Joe's...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Bubbies Mochi Ice Cream -Passion Fruit Item Code CS800119 Recalled by...
The Issue: Bubbies Mochi Ice Cream, Bubbles Cookie Dough Ice Cream Bites,Trader Joe's...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Bubbies Mochi Ice Cream -Chocolate Coconut Item Code CS812067 Recalled by...
The Issue: Bubbies Mochi Ice Cream, Bubbles Cookie Dough Ice Cream Bites,Trader Joe's...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Bubbies Mochi Ice Cream Premium Variety Pack (Strawberry Recalled by Bubbies...
The Issue: Bubbies Mochi Ice Cream, Bubbles Cookie Dough Ice Cream Bites,Trader Joe's...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Bubbies Mochi Ice Cream -Triple Chocolate Item Code CS800012 Recalled by...
The Issue: Bubbies Mochi Ice Cream, Bubbles Cookie Dough Ice Cream Bites,Trader Joe's...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Bubbies Mochi Ice Cream -Vanilla Item Code CS800002 Recalled by Bubbies...
The Issue: Bubbies Mochi Ice Cream, Bubbles Cookie Dough Ice Cream Bites,Trader Joe's...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: RespVent Closed Suction System T-Piece Tracheostomy Adult Recalled by...
The Issue: It has been determined that some units of catheters were not tightly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci SP Camera Recalled by Intuitive Surgical, Inc. Due to Some cameras...
The Issue: Some cameras were found to have residual soil adhered to the tip of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Irrisept Wound Debridement and Cleansing System. 12 units per case. Recalled...
The Issue: Potential defect in the sterile pouch seal, which may result in a lack of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ketamine 50 mg/5 mL in 0.9% Sodium Chloride Injection for Recalled by SCA...
The Issue: Lack of Assurance of Sterility.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Remisol Advance running on hardware with Windows XP Recalled by Normand-Info...
The Issue: A patch was released for a critical remote code execution vulnerability in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bioseal Trachea Extender 1/pl 50pk/Cs Recalled by Bioseal Corporation Due to...
The Issue: The reported stress crack in the port of the swivel elbow where the flip cap...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Frozen Whole Yellow Tail Fusiler-200 Up Recalled by Foremost Foods...
The Issue: FDA product due to Salmonella were mistakenly distributed to a retail...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: XP-CR Tibial Tray - Interlok 73mm Item # 195274 Recalled by Zimmer Biomet,...
The Issue: The locking bar not fully engaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XP-XP Tibial Tray - Interlok 83 mm Item # 195759 Recalled by Zimmer Biomet,...
The Issue: The locking bar not fully engaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XP-XP Tibial Tray - Interlok 73 mm Item # 195756 Recalled by Zimmer Biomet,...
The Issue: The locking bar not fully engaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QuickGraft¿ Model # 430PST Recalled by Musculoskeletal Transplant...
The Issue: Measurement listed on the label is not taken under tension, and this would...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanguard XP Tibial Tray 83 mm Item # 195253 Recalled by Zimmer Biomet, Inc....
The Issue: The locking bar not fully engaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XP-XP Tibial Tray - Interlok 79 mm Item # 195758 Recalled by Zimmer Biomet,...
The Issue: The locking bar not fully engaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XP-XP Tibial Tray - Interlok 91mm Item # 195761 Recalled by Zimmer Biomet,...
The Issue: The locking bar not fully engaging
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.