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. 1,085 recalls have been distributed to North Carolina in the last 12 months.
Showing 15701–15720 of 54,363 recalls
Recalled Item: Tropical Trail Mix Recalled by Suntree Snack Foods, LLC Due to A customer...
The Issue: A customer notified the firm that the product contained glass pieces.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Roasted Salted Cashew Halves and Pieces Recalled by Suntree Snack Foods, LLC...
The Issue: A customer notified the firm that the product contained glass pieces.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Mountain Trail Mix Recalled by Suntree Snack Foods, LLC Due to A customer...
The Issue: A customer notified the firm that the product contained glass pieces.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Roasted Salted Cashew Halves and Pieces Recalled by Suntree Snack Foods, LLC...
The Issue: A customer notified the firm that the product contained glass pieces.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Salted Cashews Halves & Pieces Recalled by Suntree Snack Foods, LLC Due to A...
The Issue: A customer notified the firm that the product contained glass pieces.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Mountain Trail Mix Recalled by Suntree Snack Foods, LLC Due to A customer...
The Issue: A customer notified the firm that the product contained glass pieces.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Glucagon Emergency Kit for Low Blood Sugar Recalled by Eli Lilly & Company...
The Issue: SUBPOTENT DRUG: Vial contained a liquid substance, instead of the expected...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Philips Azurion Interventional Fluoroscopic X-Ray System Recalled by Philips...
The Issue: When the user presses or releases both the APC (accept) button and the Float...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Permobil TiLite Recalled by TiSport, Llc Due to Some affected wheelchairs,...
The Issue: Some affected wheelchairs, with transit tie downs, that are used as a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Azurion systems with software releases 2.1(L1) and 2.1(L2) Recalled...
The Issue: 3D-RA is a reconstruction software product that can be used with the Philips...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zeego Recalled by Siemens Medical Solutions USA, Inc Due to Software...
The Issue: Software error, the software can produce an incorrect interpretation of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIMPLEXA COVID-19 Positive Control Pack Recalled by DiaSorin Molecular LLC...
The Issue: Due to unapproved raw materials used in the manufacturing of Covid-19...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Clinician Programmer Application (CPA) model A610 Clinician Software...
The Issue: A software anomaly may occur with the clinician programmer application.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ImplantDirect Recalled by Implant Direct Sybron Manufacturing LLC Due to...
The Issue: Packaged dental implant contains a different size then the size declared on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ImplantDirect Recalled by Implant Direct Sybron Manufacturing LLC Due to...
The Issue: Packaged dental implant contains a different size then the size declared on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QuikClot Combat Gauze-For Temporary External Use To Control Traumatic...
The Issue: Lack of Packaging seal integrity may result in a sterile barrier breach.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CombiDiagnost R90 is multi-functional general R/F systems. Recalled by...
The Issue: The Aleva monitor requires certain labels to be applied, some of which are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost C90 Recalled by Philips Healthcare Due to The Aleva monitor...
The Issue: The Aleva monitor requires certain labels to be applied, some of which are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProxiDiagnost N90 is multi-functional general R/F systems. Recalled by...
The Issue: The Aleva monitor requires certain labels to be applied, some of which are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ROSA One 3.1 Brain application The device is intended for Recalled by...
The Issue: The firm has become aware of a software anomaly affecting ROSA One 3.1 Brain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.