State

North Carolina product recalls

73,376 recalls have nationwide distribution and so reach North Carolina. 10,296 additional recalls listed North Carolina specifically in their distribution scope.

What the numbers show

Total: 10,296
Critical: 1,486
Severe: 2,898
Most recent: 2026-10-07

Of the 10,296 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 2,898 (28%) are Severe.

Which agencies issued them

These figures cover only the 10,296 recalls whose distribution notice names North Carolina specifically. The 73,376 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

18926–18950 of 83672

HighFDA (Drugs)·D-0458-2023·2023-03-22
Alprazolam Tablets Recalled for Potential Cross-Contamination Risk
Breckenridge Pharmaceuticals is recalling Alprazolam Tablets, USP 0.25mg distributed nationwide due to a potential cross-contamination risk from manufacturing deviations.
Product
Alprazolam Tablets, USP, 0.25mg, CIV, packaged in: a) 100-count bottle (NDC 51991-0704-01), b) 500-count bottle and c) 1,000-count bottle, Rx only, Manufactured by Centaur Pharmaceuticals PVT. LTD., Hinjewadi, Pune, INDIA, Distributed by: Breckenridge Pharmaceuticals, Inc.…
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1242-2023·2023-03-22
BD Insulin Syringes Recalled for Nonsterile Condition and Infection Risk
Becton Dickinson is recalling 686,500 units of BD insulin syringes due to a nonsterile condition that may expose patients to pathogenic microorganisms and risk of infection.
Product
BD Insulin Syringes with the BD Micro-Fine IV Needle 0.5ml, 12.7mm, 28G Single Unit Scale-Insulin Syringes are designed for administering insulin in the treatment of diabetes mellitus. Catalog Number: 329461
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1247-2023·2023-03-22
TFN-Advanced Femoral Nails May Have Incorrect Length Markings
Synthes TFN-Advanced Femoral Nails labeled as 200mm may measure 170mm, and vice versa. Healthcare providers should verify actual dimensions before surgical use.
Product
TFN-Advanced Femoral Nail 12MM/125 DEG TI CANN TFNA 170MM - STERILE. Intended for temporary fixation and stabilization of proximal femur fractures. Part Number: 04.037.212S
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0469-2023·2023-03-22
Eye allergy medication recalled for out-of-specification impurity
Teva Pharmaceuticals is recalling 715,632 bottles of Clear Eyes Once Daily eye drops due to an out-of-specification impurity found during stability testing.
Product
Clear Eyes, Once Daily, Eye Allergy Itch Relief, olopatadine hydrochloride ophthalmic solution, USP, 0.2%, Antihistamine, 2.5 mL (0.085 fl oz) bottle, Sterile, Distributed by Medtech Products Inc. Tarrytown, NY 10591, A Prestige Consumer Healthcare company, Made in Israel, UPC…
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1243-2023·2023-03-22
BD Ultra-Fine Insulin Syringes Recalled Due to Nonsterile Condition
Becton Dickinson is recalling BD Ultra-Fine Insulin Syringes (Catalog Number 326719) due to a nonsterile condition that could expose patients to pathogenic microorganisms and local infection. Approximately 80,500 units distributed worldwide are affected.
Product
BD Ultra-Fine Insulin Syringe 1mL, 12.7mm, 29G-Insulin Syringes are designed for administering insulin in the treatment of diabetes mellitus. Catalog Number: 326719
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0423-2023·2023-03-22
Sheetz M.T.go Turkey Deli Sandwich recalled for undeclared sesame allergen
Sheetz Distribution Services is recalling 10,361 M.T.go Turkey Deli Sandwiches due to undeclared sesame. Consumers with sesame allergies face potential serious allergic reactions.
Product
Sheetz M.T.go! Made To Go Turkey Deli Sandwich. The products are packaged in 4.75 oz. clear, plastic clamshells with the following UPC 759465001854 (Turkey).
Category
Food
Distribution
6 states
HighFDA (Devices)·Z-1245-2023·2023-03-22
Fusion Bioline Vascular Graft recalled due to manufacturing straightness defect
Maquet Cardiovascular is recalling one Fusion Bioline Vascular Graft from lot 25162546 that failed straightness testing. The graft could reduce blood flow or cause tension, potentially leading to bleeding and pseudo-aneurysm.
Product
Fusion Bioline Vascular Graft, Part number M00201503046B0
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1258-2023·2023-03-22
Dimension Tacrolimus Diagnostic Cartridge Recalled for Measurement Imprecision
Siemens is recalling Dimension Tacrolimus diagnostic test cartridges (lots GA2286, GA3047, GA3171) due to confirmed measurement imprecision that could lead to incorrect drug dosing and potential organ failure or toxicity.
Product
Dimension Tacrolimus (TAC) Flex reagent cartridge-In vitro diagnostic test for the quantitative measurement of tacrolimus in human whole blood on the Dimension¿ clinical chemistry system SMN: 10700795 (DF207)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1257-2023·2023-03-22
Beckman Coulter Access Immunoassay Analyzers Recalled for Defective Nut Bands
Beckman Coulter is recalling approximately 4,100 laboratory immunoassay analyzers due to defective nut bands that may cause operational failures and erroneous patient test results.
Product
Access Immunoassay Systems (1) Access 2 Immunoassay Analyzer (81600N); (2) Access 2 Immunoassay Analyzer, Refurbished (386220); (3) Access 2 Immunoassay Analyzer, Refurbished (A65531) ; and (4) Access 2 Section, DxC 600i Packaged(A25640).
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1237-2023·2023-03-22
BD Ultra-Fine Insulin Syringe Recall Due to Nonsterile Manufacturing
Becton Dickinson is recalling 45,000 units of BD Ultra-Fine Insulin Syringes (catalog 326679, lot 2164338) due to nonsterile manufacturing that could expose patients to pathogenic microorganisms and local infection. Distribution was worldwide.
Product
BD Ultra-Fine Insulin Syringe 0.5mL, 6mm, 31G - Insulin Syringes are designed for administering insulin in the treatment of diabetes mellitus. Catalog Number: 326679
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1248-2023·2023-03-22
TFN Femoral Nails dimensions mislabeled, may measure 170mm or 200mm
Synthes recalled TFN-Advanced Femoral Nails because some units have incorrect dimensions: nails labeled 200mm may measure 170mm, while those labeled 170mm may measure 200mm. This dimensional mismatch could compromise surgical fixation.
Product
TFN-Advanced Femoral Nail 12MM/130 DEG TI CANN TFNA 170MM STERILE. Intended for temporary fixation and stabilization of proximal femur fractures Part Number: 04.037.242S
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0611-2023·2023-03-22
Danone YoCrunch Vanilla Yogurt recalled for undeclared wheat allergen
Danone US LLC is recalling YoCrunch Vanilla Lowfat Yogurt because the product contains undeclared wheat, which poses a risk to consumers with wheat allergies.
Product
YoCrunch Vanilla Lowfat Yogurt with M&Ms 6 oz (170g) UPC 046675000792 packaged in plastic cup with self-contained plastic dome attached on top, 12 cups per case
Category
Food
Distribution
5 states
HighFDA (Food)·F-0583-2023·2023-03-22
Celestial Seasonings Mandarin Orange Spice Tea Contains Undeclared Caffeine
Celestial Seasonings Mandarin Orange Spice herbal tea K-cups contain undeclared caffeine from black tea. The recall affects 1,844 units distributed nationwide.
Product
Celestial Seasonings Mandarin Orange Spice Herbal Tea in K-cup pods; packed 24 to a box
Category
Food
Distribution
42 states
HighFDA (Devices)·Z-1249-2023·2023-03-22
Plato 17 Microcatheter Recalled Due to Loose Particle Risk
Scientia Vascular is recalling Plato 17 Microcatheters due to manufacturing defects that may introduce loose particles into the catheter lumen, potentially causing blood vessel blockage or inflammatory reactions.
Product
Plato 17 Microcatheter: Straight Tip, PL17-160-000 ; 45 degree Tip, PL17-160-045; 90 degree Tip, PL17-160-090
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1255-2023·2023-03-22
Medical Device Apheresis Kit Recalled Due to Stress Leak Risk
Fenwal Inc is recalling 6,564 units in certain lots of Amicus apheresis kits because centrifuge packs may develop a stress leak. No illnesses or injuries have been reported.
Product
Amicus Exchange Kit Therapeutics. Component of Amicus Separator multiprocedural apheresis platform
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1250-2023·2023-03-22
Arial mobile application recalled for Android loading failures
Securitas Healthcare is recalling the Arial mobile application for Android devices because the app does not load or function properly. Users should stop using the app immediately.
Product
Arial mobile application, model #54630 and #54640 for Android devices downloaded from the Google Play Store as part of the Arial Emergency and Nurse Call system.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0422-2023·2023-03-22
Sheetz Ham Deli Sandwiches Recalled for Undeclared Sesame
Sheetz is recalling M.T.go! Ham Deli Sandwiches that may contain undeclared sesame, a common allergen. The recall affects 5,715 sandwiches in PA, MD, OH, WV, NC, and VA.
Product
Sheetz M.T.go!, Made To Go Ham Deli Sandwich. The products are packaged in 4.75 oz. clear, plastic clamshells with the following UPC 759465001847 (Ham).
Category
Food
Distribution
6 states
HighFDA (Drugs)·D-0463-2023·2023-03-22
Clobazam Tablets Recalled Due to Cross Contamination Risk
Breckenridge Pharmaceutical is recalling Clobazam 20 mg tablets (Lot #5210147, exp. 12/2023) nationwide due to potential cross contamination from manufacturing deviations.
Product
Clobazam Tablets, 20 mg, CIV, 100-count bottle, Rx only, Manufactured by Centaur Pharmaceuticals Pvt. Ltd., Pune, INDIA, Distributed by: Breckenridge Pharmaceuticals, Inc., Berlin, CT 06037, NDC 51991-901-01
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·23V188000·2023-03-22
Volvo Recalls 2023 Models for False Emergency Call System Warnings
Volvo is recalling 2023 S60, C40, XC40, V60CC, XC60, and XC90 vehicles because a false warning may mask an actual emergency call system failure.
Product
VOLVO — VOLVO S60, C40BEV, XC40, V60CC
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1262-2023·2023-03-22
da Vinci Surgical System Patient Cart Ballscrew Failure Risk
Intuitive Surgical recalls Patient Side Carts for da Vinci X and Xi surgical systems due to ballscrew failure risk. The failure could cause uncontrolled carriage movement leading to potential tissue injury during surgery. 9 units affected.
Product
Patient Side Cart, REF: 380620, with instrument arms, used as part of the da Vinci X Surgical System, REF: IS4200; Patient Side Cart, REF: 380652, with instrument arms, used as part of the da Vinci Xi Surgical System, REF: IS4000
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·23V190000·2023-03-22
Alexis Fire Equipment Recalls 2022 Fire Apparatus Due to Winch Remote Defect
Alexis Fire Equipment is recalling 2022 fire apparatus vehicles because water may enter the winch remote, causing corrosion and unintentional winch operation.
Product
ALEXIS FIRE EQUIPMENT — ALEXIS FIRE EQUIPMENT FIRE APPARATUS
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1241-2023·2023-03-22
BD Insulin Syringes Recalled for Potential Nonsterile Condition
Becton Dickinson & Company is recalling 1.17 million BD Ultra-Fine Insulin Syringes due to a nonsterile manufacturing defect that could expose patients to pathogenic microorganisms and increase infection risk.
Product
BD Ultra-Fine Insulin Syringe 1mL, 6mm, 31G-Insulin Syringes are designed for administering insulin in the treatment of diabetes mellitus. Catalog Number: 326678
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1222-2023·2023-03-22
Hair Growth Laser Comb Recalled for Missing Safety Warnings and Labels
OMM Imports' Recreo Hair Growth Laser Comb is being recalled because 1,620 units lack required safety labels, warnings, and certification documentation. Missing labels create risk for users of the Class 3R laser device.
Product
Recreo Hair Growth Laser Comb
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1259-2023·2023-03-22
Radiation Therapy Software May Not Properly Execute Heart-Protection Breath Hold
Brainlab ExacTrac Dynamic software used in charged-particle radiation therapy systems may not properly execute Deep Inspiration Breath Hold (DIBH) functionality, a heart-protection technique. The issue affects 56 systems across the United States.
Product
Brainlab ExacTrac Dynamic software, Medical Charged-Particle Radiation Therapy System, model 20910-01E and 20910-01F.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1256-2023·2023-03-22
Ambulance cot may separate due to insufficient epoxy in assemblies
Stryker's Power-PRO 2 ambulance cots may separate at head or foot due to insufficient epoxy. Four affected units in NY and VA should be removed from service immediately.
Product
Power-PRO 2 . Intended as an ambulance cot to transport a patient to or from an emergency or non-emergency location. Model: 650705550001
Category
Medical Device
Distribution
Distributed nationwide