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. 1,900 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
1,900 in last 12 months

Showing 2792127940 of 54,363 recalls

DrugMay 25, 2018· Shadow Holdings DBA Bocchi Labs

Recalled Item: Acne Shave 3 Step Shaving System Recalled by Shadow Holdings DBA Bocchi Labs...

The Issue: CGMP Deviations: products may be contaminated with bacteria.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 25, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee systems with Laird Cooling Unit for SSFD: Material Recalled by...

The Issue: Due to a defective sealing, coolant may inflow into the electrical parts of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: AXIOM Artis with Laird Cooling Unit for SSFD: Material # Recalled by Siemens...

The Issue: Due to a defective sealing, coolant may inflow into the electrical parts of...

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

Class II — Potential Health HazardOngoing
FoodMay 25, 2018· Dean Foods, Inc.

Recalled Item: Baskin Robbins Mint Chocolate Chip Recalled by Dean Foods, Inc. Due to...

The Issue: Product may contain unlabeled coconut.

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 25, 2018· Global Commodities Inc

Recalled Item: WATAN DRY FRUITS PREMIUM QUALITY NATURAL DRIED APRICOT WITH PITT Recalled by...

The Issue: Product contains high levels of undeclared sulfites (2901 ppm).

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 24, 2018· GE Healthcare, LLC

Recalled Item: Discovery IQ 2.0 20cm Recalled by GE Healthcare, LLC Due to Some CT and...

The Issue: Some CT and CT/PET systems recently installed with a GE supplied A!...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2018· GE Healthcare, LLC

Recalled Item: Discovery MI Recalled by GE Healthcare, LLC Due to Some CT and CT/PET...

The Issue: Some CT and CT/PET systems recently installed with a GE supplied A!...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2018· GE Healthcare, LLC

Recalled Item: Discovery RT labeled as: a. MID BJG Recalled by GE Healthcare, LLC Due to...

The Issue: Some CT and CT/PET systems recently installed with a GE supplied A!...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2018· GE Healthcare, LLC

Recalled Item: CT Goldseal BrightSpeed 16 PWR TIO 2 YR Recalled by GE Healthcare, LLC Due...

The Issue: Some CT and CT/PET systems recently installed with a GE supplied A!...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2018· Beckman Coulter Inc.

Recalled Item: Sorting-Drive Product Part Recalled by Beckman Coulter Inc. Due to...

The Issue: Sorting-Drive software version 4.2 (released in October 2015) introduced a...

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

Class III — Low RiskOngoing
Medical DeviceMay 24, 2018· Fort Defiance Industries, LLC

Recalled Item: FDI FORT DEFIANCE INDUSTRIES P2131 AUTOMATED FIELD STEAM STERILIZER Recalled...

The Issue: During long-term storage (i.e. military depot), the interaction of stagnant...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2018· Beckman Coulter Inc.

Recalled Item: Software Package Recalled by Beckman Coulter Inc. Due to Sorting-Drive...

The Issue: Sorting-Drive software version 4.2 (released in October 2015) introduced a...

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

Class III — Low RiskOngoing
Medical DeviceMay 24, 2018· Draeger Medical, Inc.

Recalled Item: Perseus A500 Anesthesia Machine Recalled by Draeger Medical, Inc. Due to The...

The Issue: The Draeger anesthesia device may be able to dose 100% N2O. In the event of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2018· Beckman Coulter Inc.

Recalled Item: Sorting-Drive Professional Part Recalled by Beckman Coulter Inc. Due to...

The Issue: Sorting-Drive software version 4.2 (released in October 2015) introduced a...

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

Class III — Low RiskOngoing
Medical DeviceMay 24, 2018· Draeger Medical, Inc.

Recalled Item: Fabius GS Tiro Anesthesia Machine Recalled by Draeger Medical, Inc. Due to...

The Issue: The Draeger anesthesia device may be able to dose 100% N2O. In the event of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2018· Draeger Medical, Inc.

Recalled Item: Fabius GS MRI Anesthesia Machine Recalled by Draeger Medical, Inc. Due to...

The Issue: The Draeger anesthesia device may be able to dose 100% N2O. In the event of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2018· Beckman Coulter Inc.

Recalled Item: Software Package Recalled by Beckman Coulter Inc. Due to Sorting-Drive...

The Issue: Sorting-Drive software version 4.2 (released in October 2015) introduced a...

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

Class III — Low RiskOngoing
Medical DeviceMay 24, 2018· Draeger Medical, Inc.

Recalled Item: Apollo Anesthesia Machine Recalled by Draeger Medical, Inc. Due to The...

The Issue: The Draeger anesthesia device may be able to dose 100% N2O. In the event of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 24, 2018· Beckman Coulter Inc.

Recalled Item: Software Package Recalled by Beckman Coulter Inc. Due to Sorting-Drive...

The Issue: Sorting-Drive software version 4.2 (released in October 2015) introduced a...

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

Class III — Low RiskOngoing
Medical DeviceMay 24, 2018· Beckman Coulter Inc.

Recalled Item: Intelligent Peri-Analytical Workstation (HW+SW) Recalled by Beckman Coulter...

The Issue: Sorting-Drive software version 4.2 (released in October 2015) introduced a...

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

Class III — Low RiskOngoing