State

North Carolina product recalls

73,100 recalls have nationwide distribution and so reach North Carolina. 10,294 additional recalls listed North Carolina specifically in their distribution scope.

What the numbers show

Total: 10,294
Critical: 1,486
Severe: 2,536
Most recent: 2026-09-23

Of the 10,294 recalls naming North Carolina we have scored against our rubric, 1,486 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,536 (25%) are Severe.

Which agencies issued them

These figures cover only the 10,294 recalls whose distribution notice names North Carolina specifically. The 73,100 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

9676–9700 of 83394

SevereFDA (Food)·F-0105-2025·2024-11-13
Gordon Food Service Hawaiian Rolls Recalled for Undeclared Sesame
Perfection Bakeries is recalling Gordon Food Service Hawaiian Pull-Apart Dinner Rolls due to undeclared sesame. The recall affects 61,658 cases distributed across 12 states; consumers with sesame allergies should not consume the product.
Product
Gordon Food Service Hawaiian Pull-Apart Dinner Rolls Unsliced 1.25 Ounce. 10 unlabeled 12CT PKGS per sale unit case, product code 7148. Net. Wt. 9lbs. 6oz.
Category
Food
Distribution
12 states
SevereFDA (Food)·F-0099-2025·2024-11-13
Aunt Millie's Bakehouse Hawaiian Hamburger Buns Recalled for Undeclared Sesame
Aunt Millie's Bakehouse Hawaiian Hamburger Buns contain undeclared sesame and are being recalled by Perfection Bakeries LLC. The Class I recall affects 6,400 cases distributed across 12 states.
Product
Aunt Millie s Bakehouse Hawaiian Hamburger Buns 4.5" Sliced 3 OUNCE. 6 unlabeled 12CT PKGS per sale unit case, product code 7430. Net Wt. 13lb 8oz.
Category
Food
Distribution
12 states
HighFDA (Food)·F-0106-2025·2024-11-13
MyChai Chai Tea Concentrate Recalled for pH Control and Documentation Issues
MyChai Chai Tea Concentrate Original is recalled nationwide. The FDA found pH levels above 4.1 and missing production records.
Product
MyChai Chai Tea Concentrate Original. Product is packaged in plastic (HDPE) 1/2gallon bottle, cap has a foil liner that is induction sealed during the bottling process. Shelf stable 3 year expiration from date of manufacture. Ingredients: Water, Sugar, Organic Black Tea, Organ
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0309-2025·2024-11-13
DeRoyal Surgical Procedure Pack Smoke Evacuation Pencil Recalled
DeRoyal is recalling surgical procedure pack products containing a Stryker SafeAir Smoke Evacuation Pencil that may activate without manual input or remain active after buttons are released. The malfunction poses a risk of injury during surgical procedures.
Product
DeRoyal CHILDREN'S LAPTRACEPACK, 89-9362.06
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0039-2025·2024-11-13
FDA Recalls Regadenoson Injection for Missing Label Information
Baxter Healthcare Corporation is recalling 60,594 units of Regadenoson Injection nationwide due to missing label information on affected lot numbers. Healthcare providers with affected lots should contact the manufacturer for replacement supplies.
Product
REGADENOSON — REGADENOSON (REGADENOSON)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0286-2025·2024-11-13
epoc BGEM BUN Test Cards recalled for sodium measurement bias
Siemens recalled epoc BGEM BUN Test Cards for a negative sodium bias occurring approximately 2 months before expiration, with maximum observed bias of -10 mmol/L. No adverse events reported.
Product
epoc BGEM BUN Test Card (25 pk) for the epoc Blood Analysis System, SMN 10736515
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0107-2025·2024-11-13
MyChai Chai Tea Concentrate recalled for improper pH and missing production records
My Chai Inc is recalling MyChai Chai Tea Concentrate KALI nationwide because pH levels were found above 4.1 and production records are missing. Consumers should not consume the product.
Product
MyChai Chai Tea Concentrate KALI, 68 fl. oz. Product is packaged in plastic (HDPE) 1/2gallon bottle, cap has a foil liner that is induction sealed during the bottling process. Shelf stable 3 year expiration from date of manufacture Ingredients: Water, Sugar, Organic Black Tea Ex
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0318-2025·2024-11-13
GE Healthcare Centricity Viewer Security Vulnerability Could Allow Unauthorized Access
GE Healthcare's Centricity Universal Viewer Zero Footprint medical imaging software contains a security vulnerability that could allow unauthorized access and patient data manipulation. Approximately 120 units are affected worldwide.
Product
GE Healthcare Centricity Universal Viewer Zero Footprint, Model Numbers: 1) 2089507-083, GDZH-JINWAN-Centricity 2) 2089507-093, 10510-3-Centricity Universal Viewer Zero Footprint / ZFP-02268286, 10510-3-Centricity Universal Viewer Zero Footprint / ZFP-02030900, 1495-1-Centric
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0041-2025·2024-11-13
Generic Ibuprofen 800mg Recalled Due to Failed Impurity and Degradation Specifications
Direct Rx is recalling 1,410 bottles of Ibuprofen 800mg tablets distributed nationwide due to failed impurity specifications discovered during 18-month stability testing.
Product
Ibuprofen 800mg, Generic for: Motrin, Each tablet contains: Ibuprofen, USP 800 mg, Packaged and Distributed by: DIRECT Rx, Dawsonville, GA 30534, Mfg By: Dr. Reddy's Laboratories LA, LLC, Shreveport, LA 71106, a) NDC 61919-0621-15 (15 count bottles), b) NDC 61919-0621-30 (30 cou
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·F-0098-2025·2024-11-13
Hammond's Dark Chocolate Waffle Cones Recalled for Undeclared Milk Allergen
Hammond's Candies is recalling Dark Chocolate Filled Mini Waffle Cones nationwide due to undeclared milk allergen. Consumers with milk allergies should not consume this product.
Product
Hammond's Dark Chocolate Filled Mini Waffle Cones, packaged in a 4 oz (113g) Stand-Up Resealable Pouch. Item Number: FC23212; UPC 6 91355 90513 5. Label declares ***CONTAINS: WHEAT, SOY, TREE NUTS (COCONUT)***PACKAGED IN A FACILITY THAT PROCESSES EGG, MILK, MUSTARD, PEANUTS, SE
Category
Food
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0036-2025·2024-11-13
Morphine Sulfate Extended-Release Tablets Recalled for Impurities and Degradation
Dr. Reddy's Laboratories is recalling Morphine Sulfate Extended-Release Tablets 15 mg nationwide due to failed impurity and degradation specifications. Patients taking affected lots should contact their healthcare provider immediately.
Product
Morphine Sulfate Extended-Release Tablets 15 mg, 100-count per bottle, Rx Only, Manufactured by Mayne Pharma, Greenville, NC 27834, NDC 51862-185-01.
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0307-2025·2024-11-13
DeRoyal Children's Surgical Pack Recalled for Smoke Pencil Malfunction
DeRoyal is recalling certain lots of children's surgical procedure packs due to reports that the included Stryker smoke evacuation pencil may activate without manual input or remain active after buttons are released.
Product
DeRoyal CHILDREN'S GENERAL TRACEPACK, REF 89-9342-06
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0285-2025·2024-11-13
Endoscopic Vessel Harvesting System Recalled for Assembly Defect
Zimmer recalls the Venapax XL endoscopic vessel harvesting system due to assembly defects that may cause endoscope interference during surgery. A Gen 5 tail piece was incorrectly assembled to Gen 4 devices, affecting 432 units nationwide.
Product
Saphena Medical Venapax XL- Endoscopic Vessel Harvesting System for use in minimally invasive surgery allowing access for vessel harvesting and is primarily indicated for patients undergoing endoscopic surgery for arterial bypass. Item Number: VPX4000 (7273)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0308-2025·2024-11-13
DeRoyal Children's Orthopedic Tracepack Smoke Evacuation Pencil Malfunction Recall
DeRoyal is recalling 384 units of Children's Orthopedic TracePacks containing a Stryker smoke evacuation pencil that may activate unexpectedly or fail to deactivate, posing a burn risk during surgery.
Product
DeRoyal CHILDREN'S ORTHOPEDIC TRACEPACK, 89-9349-06
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0306-2025·2024-11-13
DeRoyal C-Section Tracepack Recall Due to Stryker Smoke Evacuation Pencil Defect
DeRoyal is recalling C-Section Tracepacks containing a Stryker SafeAir Smoke Evacuation Pencil that may activate without manual input or remain active after buttons are released.
Product
DeRoyal C-SECTION TRACEPACK, REF 89-9338-06
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0037-2025·2024-11-13
Morphine Sulfate Extended-Release Tablets Recalled for Failed Impurities Specification
Dr. Reddy's Laboratories is recalling Morphine Sulfate Extended-Release Tablets 30 mg (Lot FG13996) nationwide due to failed impurities and degradation specifications.
Product
Morphine Sulfate Extended-Release Tablets 30 mg, 100-count bottles, Rx Only, Manufactured by Mayne Pharma, Greenville, NC 27834, NDC 51862-186-01.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0119-2025·2024-11-13
Oregon Orchards Banana Smoothie Mix recalled for inadequate acidification documentation
My Chai Inc is recalling Oregon Orchards Banana Smoothie Mix nationwide due to insufficient production records proving proper acidification. Consumers should not consume the product.
Product
Oregon Orchards Banana Smoothie Mix. Product is packaged in the same square 0.5gallon HDPE plastic bottles and the volume is 68 fl oz. Ingredients: Sugar, banana puree, water, natural flavor, citric acid, xanthan gum, sodium benzoate (to help protect flavor-1/10 of 1%), vanilla
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0316-2025·2024-11-13
X-ray System Software May Fail to Display Images During Mode Switching
SHIMADZU CORPORATION's SONIALVISION G4 X-ray system may occasionally fail to display images when switching from fluoroscopy to radiography mode. This could result in examination delays or cancellations.
Product
SONIALVISION G4 is a multi-purpose X-ray R/F system. The equipment is suitable for radiographic and fluoroscopic examinations, including general radiography and pediatric examinations, excluding mammography.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0111-2025·2024-11-13
MySyrup Sugar Free Almond Syrup Recalled for Missing Production Records
My Chai Inc is recalling MySyrup Sugar Free Almond Syrup due to missing production records. The recall affects 212 jugs with batch numbers and expiration dates from August 2023 through December 2024.
Product
MySyrup Sugar Free Almond Syrup. Product is packaged in the same square 0.5gallon HDPE plastic bottles and the volume is 68 fl oz. Ingredients: Water, natural flavor, Madagascar vanilla extract, sodium benzoate and potassium sorbate (to protect flavor), sucralose, acesulfame pot
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0038-2025·2024-11-13
Dapsone Gel 7.5% recalled nationwide due to crystallization
Viona Pharmaceuticals is recalling Dapsone Gel 7.5% due to crystallization. The voluntary recall covers 6,048 pumps distributed nationwide in the United States.
Product
DAPSONE — DAPSONE (DAPSONE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0315-2025·2024-11-13
Biocare Medical Recalls IHC Kits Due to Potential Staining Failure
Biocare Medical is recalling specific IHC kits containing DAB Buffer because they may produce weak or no staining, leading to test failure.
Product
intelliPATH Universal HRP Detection Kit, REF: IPK5011G80, containing DAB Buffer, Catalog Number: IPBF5009G20; ONCORE Pro DAB Chromogen, REF: OPRI6056KT180, containing DAB Buffer, Catalog Number: OPRI6055T60; IP DAB Chromogen Kit 80 ml, REF: IPK5010G80, containing DAB Buffer,
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0317-2025·2024-11-13
Shimadzu FLUOROspeed X-ray System Software Recall for Image Display Failure
Shimadzu is recalling 30 FLUOROspeed X-ray systems because software may fail to display images when switching modes, potentially delaying or canceling examinations.
Product
The FLUOROspeed is intended to be used as a universal diagnostic imaging system for radiographic and fluoroscopic studies. Using a flat detector, it can perform a range of applications including general R/F, angiography and pediatric examinations. FLUOROspeed may be used for emer
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0114-2025·2024-11-13
MySyrup Sugar Free Hazelnut Syrup Recalled Due to Missing Production Records
MySyrup Sugar Free Hazelnut Syrup (556 jugs) is being recalled nationwide because production records are missing for this acidified product, preventing verification of proper processing procedures.
Product
MySyrup Sugar Free Hazelnut Syrup. Product is packaged in the same square 0.5gallon HDPE plastic bottles and the volume is 68 fl oz. Ingredients: Water, natural and artificial flavor, potassium sorbate and sodium benzoate (to protect flavor), sucralose, acesulfame potassium, cit
Category
Food
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0314-2025·2024-11-13
Adult Cap-ONE Biteblock devices recalled for expired product distribution
Nihon Kohden America Inc is recalling 17 Adult Cap-ONE Biteblock devices shipped after expiration dates. The single-use devices are intended for sampling CO2 and administering oxygen during endoscopy procedures.
Product
Adult Cap-ONE Biteblock REF YG-227T The cap-ONE Biteblock is intended to sample CO2 and administer supplemental oxygen, for patients who can wear a 20mm bite block, during endoscopy type procedures. The device is intended for single patient use only.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0284-2025·2024-11-13
Canon Medical PET-CT System Software Malfunction Prevents Image Reconstruction
27 Canon Cartesion Prime PET-CT imaging systems may experience software processing failures during simultaneous imaging of multiple patients, necessitating repeat examinations. The issue occurs when PET acquisition or reconstruction for another patient is performed while reconstruction is in progress.
Product
Cartesion Prime, Digital PET-CT, Model: PCD-1000A/3D.004, PCD-1000A/3D, is a diagnostic imaging system that combines Positron Emission Tomography (PET) and X-ray Computed Tomography (CT) systems.
Category
Medical Device
Distribution
18 states