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. 1,098 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
1,098 in last 12 months

Showing 11161–11180 of 54,363 recalls

DrugDecember 23, 2022· GFA Production Xiamen Co. Ltd.

Recalled Item: CVS First Aid Home Recalled by GFA Production Xiamen Co. Ltd. Due to...

The Issue: Microbial Contamination of Non-Sterile Products: FDA Laboratory results...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 23, 2022· GFA Production Xiamen Co. Ltd.

Recalled Item: Easy Care First Aid 10 Person 2009 ANSI Recalled by GFA Production Xiamen...

The Issue: Microbial Contamination of Non-Sterile Products: FDA Laboratory results...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 23, 2022· GFA Production Xiamen Co. Ltd.

Recalled Item: Adventure First Aid 1.5 Recalled by GFA Production Xiamen Co. Ltd. Due to...

The Issue: Microbial Contamination of Non-Sterile Products: FDA Laboratory results...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 23, 2022· GFA Production Xiamen Co. Ltd.

Recalled Item: Easy Care First Aid 25 Person 2009 ANSI Recalled by GFA Production Xiamen...

The Issue: Microbial Contamination of Non-Sterile Products: FDA Laboratory results...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 23, 2022· GFA Production Xiamen Co. Ltd.

Recalled Item: Easy Care First Aid 10 Person 2009 ANSI Recalled by GFA Production Xiamen...

The Issue: Microbial Contamination of Non-Sterile Products: FDA Laboratory results...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 23, 2022· GFA Production Xiamen Co. Ltd.

Recalled Item: Adventure First Aid 1.0 Recalled by GFA Production Xiamen Co. Ltd. Due to...

The Issue: Microbial Contamination of Non-Sterile Products: FDA Laboratory results...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 23, 2022· GFA Production Xiamen Co. Ltd.

Recalled Item: Easy Care first aid Burn Cream (benzalkonium chloride 0.13% and Recalled by...

The Issue: Microbial Contamination of Non-Sterile Products: FDA Laboratory results...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceDecember 23, 2022· Philips Healthcare (Suzhou) Co., Ltd.

Recalled Item: Incisive CT Recalled by Philips Healthcare (Suzhou) Co., Ltd. Due to...

The Issue: Multiple software issues which have the potential to lead to misdiagnosis...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2022· Getinge Usa Sales Inc

Recalled Item: Getinge Flow-e Anesthesia System Recalled by Getinge Usa Sales Inc Due to...

The Issue: Due to a software bug, under certain conditions, pressure cannot be built up...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 22, 2022· Bard Peripheral Vascular Inc

Recalled Item: The Covera Vascular Covered Stent is a flexible Recalled by Bard Peripheral...

The Issue: An increase in the reported complaint rate for inability to deploy was...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE UNITE FOOT & ANKLE DRILL BIT Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: The recall is due to observed intra-operative screw failure. When...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2022· Access Vascular, Inc

Recalled Item: HydroMID 4Fr Single Lumen Maximal Barrier Kit- Indicated for short Recalled...

The Issue: Product Mislabeled on the outer bag and inner kit Tyvek header bag

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2022· SunMed Holdings, LLC

Recalled Item: AirQ3 Self Pressurizing ILA with Automatic Cuff Inflation and GA Recalled by...

The Issue: There is an orogastric (OG) tube size discrepancy between the labeling in...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2022· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Centaur XP and ADVIA Centaur XPT Anti-HBe2 (aHBe2) 50T- Recalled by...

The Issue: Anti-HBe2 (aHBe2) interference with the Hepatitis B e Antigen (HBeAg) Assay,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2022· Maquet Cardiovascular, LLC

Recalled Item: Hemopro 2 with Vasoshield Recalled by Maquet Cardiovascular, LLC Due to...

The Issue: Ink on the Vasoshield syringe Maquet logo may chip resulting in an...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2022· Access Vascular, Inc

Recalled Item: HydroMID 4Fr Single Lumen Maximal Barrier Kit-indicated for short term...

The Issue: Label with the incorrect component listed on the inner kit Tyvek header bag

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE UNITE FOOT & ANKLE Screw Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: The recall is due to observed intra-operative screw failure. When...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE UNITE FOOT & ANKLE Screw Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: The recall is due to observed intra-operative screw failure. When...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2022· Getinge Usa Sales Inc

Recalled Item: Getinge Flow-c Anesthesia System Recalled by Getinge Usa Sales Inc Due to...

The Issue: Due to a software bug, under certain conditions, pressure cannot be built up...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 22, 2022· Getinge Usa Sales Inc

Recalled Item: Getinge Flow-i Anesthesia Systems Flow-i C20 Recalled by Getinge Usa Sales...

The Issue: Due to a software bug, under certain conditions, pressure cannot be built up...

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

Class I — Serious Health HazardOngoing