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. 1,824 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
1,824 in last 12 months

Showing 3854138560 of 54,363 recalls

Medical DeviceDecember 3, 2015· Becton Dickinson & Company

Recalled Item: BD Vacutainer PLUS K2EDTA Tubes (Plastic). 13 x 75 mm Recalled by Becton...

The Issue: Some of the Blood Collection Tubes in these lots were manufactured with...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2015· Becton Dickinson & Company

Recalled Item: BD Vacutainer PLUS K2EDTA Tubes (Plastic). 13 x 75 mm Recalled by Becton...

The Issue: Some of the Blood Collection Tubes in these lots were manufactured with...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2015· Becton Dickinson & Company

Recalled Item: BD Vacutainer PLUS K2EDTA Tubes (Plastic). 13 x 75 mm Recalled by Becton...

The Issue: Some of the Blood Collection Tubes in these lots were manufactured with...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2015· Becton Dickinson & Company

Recalled Item: BD Vacutainer PLUS K2EDTA Tubes (Plastic). 13 x 75 mm Recalled by Becton...

The Issue: Some of the Blood Collection Tubes in these lots were manufactured with...

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

Class II — Potential Health HazardOngoing
DrugDecember 2, 2015· Pfizer Inc.

Recalled Item: Norpace CR (disopyramide phosphate) extended-release capsules USP Recalled...

The Issue: Failed Dissolution Specification

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

Class III — Low RiskOngoing
Refund
FoodDecember 2, 2015· Jem Raw Chocolate, LLC

Recalled Item: Superberry Maqui Camu - Sprouted Almond Spread. Product is packaged Recalled...

The Issue: Superberry Maqui Camu - Sprouted Almond Spread is recalled because it has...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 2, 2015· Jem Raw Chocolate, LLC

Recalled Item: Cinnamon Red Maca - Sprouted Almond Spread. Product is packaged in glass...

The Issue: Cinnamon Red Maca - Sprouted Almond Spread is recalled because it has the...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 2, 2015· Jem Raw Chocolate, LLC

Recalled Item: Cashew Cardamom - Sprouted Cashew Almond Spread. Product is packaged...

The Issue: Cashew Cardamom - Sprouted Cashew Almond Spread is recalled because it has...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 2, 2015· Jem Raw Chocolate, LLC

Recalled Item: Coconut Cardamom - Sprouted Almond Spread. Product is packaged in glass jars...

The Issue: Coconut Cardamom- Sprouted Almond Spread is recalled because it has the...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 2, 2015· Jem Raw Chocolate, LLC

Recalled Item: Hazelnut Raw Cacao - Sprouted Hazelnut Spread. Product is packaged in glass...

The Issue: Hazelnut Raw Cacao - Sprouted Hazelnut Spread is recalled because it has the...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceDecember 2, 2015· Medtronic

Recalled Item: Best Practice Kits containing certain production lots of Endo GIA Recalled...

The Issue: Staplers fail to fire or partially fire and reports of the instrument...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2015· Gsi Group Inc

Recalled Item: PRN 50-M+ Recalled by Gsi Group Inc Due to The item was recalled due to an...

The Issue: The item was recalled due to an increased user/patient risk of exposure to...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2015· Medtronic

Recalled Item: Covidien Endo GIA Ultra Universal 12 mm Short Stapler Handle Recalled by...

The Issue: Staplers fail to fire or partially fire and reports of the instrument...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2015· Medtronic

Recalled Item: Covidien Endo GIA Ultra Universal 12 mm XL Stapler Handle Recalled by...

The Issue: Staplers fail to fire or partially fire and reports of the instrument...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2015· Medtronic

Recalled Item: Covidien Endo GIA Ultra Universal Standard Stapler Handle Recalled by...

The Issue: Staplers fail to fire or partially fire and reports of the instrument...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2015· Skytron, Div. The KMW Group, Inc

Recalled Item: Ergon 2 Articulating Equipment Boom Monitor Brackets mounting point for...

The Issue: The hardware that holds the VESA plate and the display interface / monitor...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2015· Biomet, Inc.

Recalled Item: Black Mamba Suture Passer Recalled by Biomet, Inc. Due to There may be a...

The Issue: There may be a separation and an insufficient weld between the spring and...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 2, 2015· Biomet, Inc.

Recalled Item: Green Mamba Suture Passer Recalled by Biomet, Inc. Due to There may be a...

The Issue: There may be a separation and an insufficient weld between the spring and...

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

Class II — Potential Health HazardOngoing
FoodDecember 1, 2015· Reser's Fine Foods Inc.

Recalled Item: Winn Dixie Old Fashioned Potato Salad Recalled by Reser's Fine Foods Inc....

The Issue: Possible Listeria monocytogenes contamination.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 1, 2015· Microbiologics Inc

Recalled Item: QC Sets and Panels: KWIK-STIK Cepheid Smart GBS QC Set Recalled by...

The Issue: The Lactobacillus acidophilus negative control (item 0243 single KWIK-STIK)...

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

Class II — Potential Health HazardOngoing