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. 2,828 recalls have been distributed to North Carolina in the last 12 months.
Showing 2281–2300 of 54,363 recalls
Recalled Item: Intera 1.5T Achieva Nova-Dual Product Number: 781173 Recalled by Philips...
The Issue: identified an issue where a component failure in the specific Gradient Coil...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Explorer/Nova Dual Product Number: 781108 Recalled by Philips...
The Issue: identified an issue where a component failure in the specific Gradient Coil...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartPath to dStream for 1.5T¿ Recalled by Philips North America Due to...
The Issue: identified an issue where a component failure in the specific Gradient Coil...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Achieva IT Nova Product Number: 781175 Recalled by Philips North...
The Issue: identified an issue where a component failure in the specific Gradient Coil...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Achieva Nova Product Number: 781172 Recalled by Philips North...
The Issue: identified an issue where a component failure in the specific Gradient Coil...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera Achieva 1.5T Pulsar Recalled by Philips North America Due to...
The Issue: identified an issue where a component failure in the specific Gradient Coil...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Master/Nova Product Number: 781106 Recalled by Philips North...
The Issue: identified an issue where a component failure in the specific Gradient Coil...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 1.5T Omni/Stellar Recalled by Philips North America Due to identified...
The Issue: identified an issue where a component failure in the specific Gradient Coil...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva XR Product Numbers: (1) 781153 Recalled by Philips North America Due...
The Issue: identified an issue where a component failure in the specific Gradient Coil...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ketorolac Tromethamine Ophthalmic Solution Recalled by Apotex Corp. Due to...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Azelastine HCl Ophthalmic Solution Recalled by Apotex Corp. Due to Lack of...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DOBUTamine Injection Recalled by Pfizer Inc. Due to Discoloration;...
The Issue: Discoloration; discolored solution from cracked vials
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution Recalled by Apotex...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lacosamide Oral Solution Recalled by Apotex Corp. Due to Defective...
The Issue: Defective Container: This recall is being initiated due to a leaking unit...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Philips eL18-4 EMT Transducer. Recalled by Philips Ultrasound, Inc Due to...
The Issue: Ultrasound transducer devices were beyond their useful life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips C9-5EC Transducer. Recalled by Philips Ultrasound, Inc Due to...
The Issue: Ultrasound transducer devices were beyond their useful life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips eL18-4 Transducer. Recalled by Philips Ultrasound, Inc Due to...
The Issue: Ultrasound transducer devices were beyond their useful life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips C5-2 Transducer. Recalled by Philips Ultrasound, Inc Due to...
The Issue: Ultrasound transducer devices were beyond their useful life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips L12-3 Transducer. Recalled by Philips Ultrasound, Inc Due to...
The Issue: Ultrasound transducer devices were beyond their useful life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips X6-1 Transducer. Recalled by Philips Ultrasound, Inc Due to...
The Issue: Ultrasound transducer devices were beyond their useful life.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.