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. 1,924 recalls have been distributed to North Carolina in the last 12 months.

54,363 total recalls
1,924 in last 12 months

Showing 2220122220 of 54,363 recalls

DrugSeptember 19, 2019· Torrent Pharma Inc.

Recalled Item: Losartan Potassium/ Hydrochlorothiazide Tablets Recalled by Torrent Pharma...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 19, 2019· Torrent Pharma Inc.

Recalled Item: Losartan Potassium /Hydrochlorothiazide Tablets Recalled by Torrent Pharma...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 19, 2019· Torrent Pharma Inc.

Recalled Item: Losartan Potassium Tablets Recalled by Torrent Pharma Inc. Due to CGMP...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 19, 2019· Torrent Pharma Inc.

Recalled Item: Losartan Potassium Tablets Recalled by Torrent Pharma Inc. Due to CGMP...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 19, 2019· YTM, Inc. DBA A Priori Specialty Foods

Recalled Item: Espinaler Razor Clams (Trimmed) 4/6 Classic Line Recalled by YTM, Inc. DBA A...

The Issue: An unknown object was found in a tin

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 19, 2019· Ra Medical Systems, Inc.

Recalled Item: Ra Medical Systems DABRA Catheter 5F (1.5mm) Recalled by Ra Medical Systems,...

The Issue: The firm has become aware there is a potential problem with its DABRA...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2019· Pacific Medical Group Inc.

Recalled Item: Pacific Medical GE Corometrics Nautilus Ultrasound Transducer w/wing 5700LAX...

The Issue: Fetal transducers distributed in advance of receiving 510(k) and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2019· Pacific Medical Group Inc.

Recalled Item: Pacific Medical GE Corometrics Nautilus Ultrasound Transducer w/knob...

The Issue: Fetal transducers distributed in advance of receiving 510(k) and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2019· Pacific Medical Group Inc.

Recalled Item: Pacific Medical Philips M1355A Toco Transducer with belt wire/knob Recalled...

The Issue: Fetal transducers distributed in advance of receiving 510(k) and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2019· Pacific Medical Group Inc.

Recalled Item: Pacific Medical Philips M1356A Ultrasound Transducer with belt/wire knob...

The Issue: Fetal transducers distributed in advance of receiving 510(k) and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2019· Pacific Medical Group Inc.

Recalled Item: Pacific Medical GE Corometrics Nautilus Toco Transducer w/wing (2264LAX)...

The Issue: Fetal transducers distributed in advance of receiving 510(k) and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2019· Pacific Medical Group Inc.

Recalled Item: Pacific Medical GE Corometrics Nautilus Toco Transducer w/knob Recalled by...

The Issue: Fetal transducers distributed in advance of receiving 510(k) and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2019· Pacific Medical Group Inc.

Recalled Item: Pacific Medical GE Corometrics Nautilus Ultrasound Recalled by Pacific...

The Issue: Fetal transducers distributed in advance of receiving 510(k) and...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2019· CrossRoads Extremity Systems, LLC

Recalled Item: MotoBand CP Recalled by CrossRoads Extremity Systems, LLC Due to Potentially...

The Issue: Potentially includes a 3.0mm x 30mm screw instead of 3.0mm x 28mm screw.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2019· Philips Medical Systems (Cleveland) Inc

Recalled Item: Forte Gamma Camera System is intended to produce images depicting Recalled...

The Issue: An issue with the Detector for the Forte Family of cameras may result in...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 19, 2019· Philips Medical Systems (Cleveland) Inc

Recalled Item: Forte Gamma Camera System is intended to produce images depicting Recalled...

The Issue: An issue with the Detector for the Forte Family of cameras may result in...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 19, 2019· Philips Medical Systems (Cleveland) Inc

Recalled Item: Forte Gamma Camera System is intended to produce images depicting Recalled...

The Issue: An issue with the Detector for the Forte Family of cameras may result in...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 19, 2019· Philips Medical Systems (Cleveland) Inc

Recalled Item: Forte Gamma Camera System is intended to produce images depicting Recalled...

The Issue: An issue with the Detector for the Forte Family of cameras may result in...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 19, 2019· Philips Medical Systems (Cleveland) Inc

Recalled Item: Forte Gamma Camera System is intended to produce images depicting Recalled...

The Issue: An issue with the Detector for the Forte Family of cameras may result in...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 19, 2019· Baxter Healthcare Corporation

Recalled Item: TherMax Blood Warmer Unit Recalled by Baxter Healthcare Corporation Due to...

The Issue: TherMax Blood Warmers may not be in compliance with an electrical safety...

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

Class II — Potential Health HazardOngoing