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 6401–6420 of 29,737 recalls

Medical DeviceMay 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...

The Issue: Potential for the labeled sterile ultrasound gel component within packs to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...

The Issue: Potential for the labeled sterile ultrasound gel component within packs to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...

The Issue: Potential for the labeled sterile ultrasound gel component within packs to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...

The Issue: Potential for the labeled sterile ultrasound gel component within packs to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...

The Issue: Potential for the labeled sterile ultrasound gel component within packs to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2023· GE OEC Medical Systems, Inc

Recalled Item: OEC Flexiview 8800 Systems with 9-inch Image Intensifier Recalled by GE OEC...

The Issue: Image intensifiers on systems, used to provide fluoroscopic/digital spot...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...

The Issue: Potential for the labeled sterile ultrasound gel component within packs to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...

The Issue: Potential for the labeled sterile ultrasound gel component within packs to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...

The Issue: Potential for the labeled sterile ultrasound gel component within packs to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...

The Issue: Potential for the labeled sterile ultrasound gel component within packs to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...

The Issue: Potential for the labeled sterile ultrasound gel component within packs to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...

The Issue: Potential for the labeled sterile ultrasound gel component within packs to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...

The Issue: Potential for the labeled sterile ultrasound gel component within packs to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Custom Sterile and Non-Sterile Procedural Kits containing Turkuaz Ultrasound...

The Issue: Potential for the labeled sterile ultrasound gel component within packs to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2023· Full Vision Inc

Recalled Item: TRACKMASTER Recalled by Full Vision Inc Due to Treadmill malfunction: drive...

The Issue: Treadmill malfunction: drive PCB can misread the signals and stop or reverse...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2023· Full Vision Inc

Recalled Item: TRACKMASTER Recalled by Full Vision Inc Due to Treadmill malfunction: drive...

The Issue: Treadmill malfunction: drive PCB can misread the signals and stop or reverse...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2023· Full Vision Inc

Recalled Item: TRACKMASTER Recalled by Full Vision Inc Due to Treadmill malfunction: drive...

The Issue: Treadmill malfunction: drive PCB can misread the signals and stop or reverse...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2023· Full Vision Inc

Recalled Item: TRACKMASTER Recalled by Full Vision Inc Due to Treadmill malfunction: drive...

The Issue: Treadmill malfunction: drive PCB can misread the signals and stop or reverse...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2023· Full Vision Inc

Recalled Item: TRACKMASTER Recalled by Full Vision Inc Due to Treadmill malfunction: drive...

The Issue: Treadmill malfunction: drive PCB can misread the signals and stop or reverse...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2023· Boston Scientific Neuromodulation Corporation

Recalled Item: Driver Instrument Recalled by Boston Scientific Neuromodulation Corporation...

The Issue: Pending update to indirect decompression system instructions for use...

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

Class II — Potential Health HazardOngoing