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. 1,117 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
1,117 in last 12 months

Showing 9121–9140 of 54,363 recalls

Medical DeviceJune 5, 2023· Luminex Corporation

Recalled Item: VERIGENE Clostridium difficile Nucleic Acid Test Recalled by Luminex...

The Issue: It is possible that in rare instances the VERIGENE CDF Nucleic Acid Test Kit...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2023· Siemens Medical Solutions USA, Inc

Recalled Item: Cios Select VA 21 with FD- A Mobile X-ray system Recalled by Siemens Medical...

The Issue: Incorrect glue was applied on the plexiglass sheet on the single tank cover...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 5, 2023· Datascope Corp.

Recalled Item: Cardiosave Rescue Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...

The Issue: IABP may lose the ability to charge batteries in one or both bay slots....

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 5, 2023· Datascope Corp.

Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...

The Issue: An unexpected shutdown of the IABP may occur due to failures of tantalum...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 2, 2023· Covidien, LLC

Recalled Item: Covidien Cytosponge Cell Collection Device Recalled by Covidien, LLC Due to...

The Issue: Cell Collection Device may be at increased risk of the sponge detaching from...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2023· Megadyne Medical Products, Inc.

Recalled Item: MEGADYNE MEGA SOFT Dual Reusable Patient Return Electrode. used during...

The Issue: Firm has received reports of patient burns in surgical procedures where...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 1, 2023· Siemens Healthcare Diagnostics Inc

Recalled Item: epoc BGEM BUN Test Card with epoc Host SW v3.37.3 Recalled by Siemens...

The Issue: There is potential for discrepant high glucose results in samples with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2023· Siemens Healthcare Diagnostics Inc

Recalled Item: epoc BGEM Test Card (BUN & TCO2) Recalled by Siemens Healthcare Diagnostics...

The Issue: There is potential for discrepant high glucose results in samples with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2023· Siemens Healthcare Diagnostics Inc

Recalled Item: epoc BGEM Crea Test Card with epoc Host SW v3.37.3 Recalled by Siemens...

The Issue: There is potential for discrepant high glucose results in samples with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2023· Megadyne Medical Products, Inc.

Recalled Item: MEGADYNE MEGA SOFT Universal Dual Patient Return Electrode. used during...

The Issue: Firm has received reports of patient burns in surgical procedures where...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 1, 2023· Megadyne Medical Products, Inc.

Recalled Item: MEGADYNE MEGA SOFT Universal Plus Patient Return Electrode. used during...

The Issue: Firm has received reports of patient burns in surgical procedures where...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 1, 2023· Megadyne Medical Products, Inc.

Recalled Item: MEGADYNE MEGA SOFT Pediatric Patient Return Electrode. used during...

The Issue: Firm has received reports of patient burns in surgical procedures where...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 1, 2023· Megadyne Medical Products, Inc.

Recalled Item: MEGADYNE MEGA 2000 Patient Return Electrode. used during electrosurgery...

The Issue: Firm has received reports of patient burns in surgical procedures where...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 1, 2023· Megadyne Medical Products, Inc.

Recalled Item: MEGADYNE MEGA SOFT Reusable Patient Return Electrode. used during...

The Issue: Firm has received reports of patient burns in surgical procedures where...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 1, 2023· Megadyne Medical Products, Inc.

Recalled Item: MEGADYNE MEGA SOFT Universal Plus Dual Patient Return Electrode. used...

The Issue: Firm has received reports of patient burns in surgical procedures where...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 1, 2023· Megadyne Medical Products, Inc.

Recalled Item: MEGADYNE MEGA SOFT Universal Patient Return Electrode. used during...

The Issue: Firm has received reports of patient burns in surgical procedures where...

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

Class I — Serious Health HazardOngoing
FoodJune 1, 2023· Amin Trading Agency LLC

Recalled Item: Everest Sambhar Masala Recalled by Amin Trading Agency LLC Due to Potential...

The Issue: Product may be contaminated with Salmonella

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 1, 2023· Amin Trading Agency LLC

Recalled Item: Everest Garam Masala Recalled by Amin Trading Agency LLC Due to Potential...

The Issue: Product may be contaminated with Salmonella

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 1, 2023· Amin Trading Agency LLC

Recalled Item: Maggi Masala ae Magic Recalled by Amin Trading Agency LLC Due to Potential...

The Issue: Product may be contaminated with Salmonella

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 31, 2023· The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Recalled Item: ZIPRASIDONE HYDROCHLORIDE CAPSULES 20 mg Recalled by The Harvard Drug Group...

The Issue: Labeling: Label Mix-up: Unit Dose cartons labeled as Ziprasidone...

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

Class I — Serious Health HazardOngoing
Refund