State

North Carolina product recalls

72,940 recalls have nationwide distribution and so reach North Carolina. 10,261 additional recalls listed North Carolina specifically in their distribution scope.

What the numbers show

Total: 10,261
Critical: 1,476
Severe: 2,520
Most recent: 2026-09-09

Of the 10,261 recalls naming North Carolina we have scored against our rubric, 1,476 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,520 (25%) are Severe.

Which agencies issued them

These figures cover only the 10,261 recalls whose distribution notice names North Carolina specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

4351–4375 of 83201

HighFDA (Devices)·Z-0584-2026·2025-12-03
Blood lead test kits recalled over mislabeled calibration buttons
Magellan Diagnostics is recalling 1,774 LeadCare II Blood Lead Test Kits because calibration buttons used in kitting were labelled with the wrong lot number.
Product
The LeadCare¿ II Blood Lead Test System relies on electrochemistry and a unique Sensor to detect lead in whole blood. The LeadCare¿ II Test Kit is provided with the following materials: " Sensors (2 Containers of 24 sensors each; 48 tests) " Treatment Reagent Tubes (2 packag
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0587-2026·2025-12-03
Q400 massage tables recalled over heat components that can overheat
Pivotal Health Solutions is recalling 34 Quantum Intersegmental Tables, model Q400, because damage to the heat function components can lead to overheating and smoldering.
Product
Quantum Intersegmental Table, Model/Catalog Number: Q400; heated massage table
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0601-2026·2025-12-03
Brain access devices recalled because packaging tape contains latex
Stryker is recalling 39,148 NICO BrainPath devices because tape used to secure components in the packaging contains latex despite the products being labelled latex-free.
Product
NICO BrainPath; Product Number/Product Name NN-8024 BrainPath Shephard's Hook - Greenberg; NN-8025 BrainPath Shephard's Hook - Sugita; NN-8026 BrainPath Shephard's Hook - Budde; NN-8042 BrainPath Shephard's Hook - Greenberg LK;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0594-2026·2025-12-03
Diabetes clinic software recalled over incorrect sensor glucose graph data
Medtronic MiniMed is recalling 12,126 CareLink Clinic installations because a software error displays incorrect data on the 24-hour sensor glucose overview graph.
Product
CareLink Clinic, REF: MMT-7350
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0722-2026·2025-12-03
Hot and cold wraps recalled over microwave instructions causing burns
DJO is recalling 1,594 Cold Form Wraps because the instructions tell users to microwave the wrap for three minutes, which may cause leaks or second degree burns.
Product
Cold Form Wrap: Back, REF: DP163CT03-BLK-L,XL, and Shoulder, REF: DP163CT02
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0720-2026·2025-12-03
Anesthesia vaporizers recalled over the potential for anesthesia leakage
Mindray is recalling 148 Sevoflurane V90 Electronic Vaporizers used with the A9 Anesthesia System over the potential for anesthesia leakage.
Product
Sevoflurane (SEVO) V90 Electronic Vaporizer with the A9 Anesthesia System. Labeled as the following: 1. Sev E_Vap. (Safety Filling adapter), Part Number: 115-066756-00. 2. Exchange Sev E_Vap. (Safety Filling adapter), Part Number: E115-066756-00. Product Description: Th
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0602-2026·2025-12-03
Respiratory test panels recalled over elevated risk of false negative results
BioFire Diagnostics is recalling 23 kits of the BioFire Respiratory Panel 2.1 because unintended movement of pouch chemistry may cause false negative results and control failures.
Product
BioFire Respiratory Panel 2.1, IVD, REF: 423742 (30 test kit)
Category
Medical Device
Distribution
11 states
HighFDA (Drugs)·D-0179-2026·2025-12-03
Saline nasal spray recalled over microbial contamination with Pseudomonas lactis
Medical Products Laboratories is recalling 41,328 bottles of Walgreens Saline Nasal Spray with Xylitol over microbial contamination identified as Pseudomonas lactis.
Product
Walgreens Saline Nasal Spray WITH XYLITOL, 1.5 oz (45mL) bottle, DISTRIBUTED BY: WALGREEN CO., 200 WILMOT RD., DEERFIELD, IL 60015, NDC 0363-3114-01
Category
Drug
Distribution
Distributed nationwide
HighFDA (Food)·H-0207-2026·2025-12-03
Ice cream bars recalled over undeclared wheat and soy allergens
Jeni's Splendid Ice Creams is recalling 3,767 cases of Passion Fruit Dreamsicle Ice Cream Bars over undeclared wheat and soy.
Product
Jeni's Passion Fruit Dreamsicle Ice Cream Bars, 3 FL OZ (89 ML)/9 FL OZ (266 ML), packaged 3 bars per retail carton with Item UPC: 850060644122, packed 8 retail cartons per case with Case UPC: 10850060644129
Category
Food
Distribution
10 states
ModerateFDA (Devices)·Z-0585-2026·2025-12-03
Culture media recalled over contamination that may darken the broth
Remel is recalling cation-adjusted Mueller Hinton broth and Brucella broth because the products may contain contamination, which may result in a darker or brown media color.
Product
1. CAMHB W/LHB, MANUAL, 11ML, 10/BOX YCP112-10 2. BRUCELLA BROTH, 11ML, 10/BOX YT3450
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0577-2026·2025-12-03
Cancer test reports recalled for omitting the companion diagnostic claims page
Foundation Medicine is recalling 59 FoundationOne CDx reports that were sent to customers without the companion diagnostic Claims Page.
Product
FoundationOne CDx (F1CDx), RAL-0003 version 31.0
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0724-2026·2025-12-03
Tuberculosis test cartridges recalled after failing expected stability criteria
Cepheid is recalling 9,880 Xpert MTB/RIF cartridges from one lot because product testing did not meet expected stability criteria.
Product
Xpert MTB/RIF. Model Number: GXMTB/RIF-US-10.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0581-2026·2025-12-03
Vitrectomy probe packs recalled with no reason stated in the record
Alcon Research is recalling 28,323 Constellation UltraVit 10K and HyperVit 20K vitrectomy probe packs; the enforcement record does not state a reason.
Product
CONSTELLATION ULTRAVIT 10K and CONSTELLATION HYPERVIT 20K, Description/REF: 25+ TOTALPLUS CP PAK 20K CPM BWV .9 IU/ 8065000093; 25+ TOTALPLUS CP PAK 20K CPM BV .9 IU/ 8065000095; 27+ TOTALPLUS CP PAK 20K CPM BV .9 IU/ 8065000096; 23GA BEVEL ULTRAVIT 10,000 CPM/ 8065752413; 25+ B
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25V834000·2025-12-02
Zero Recalls 2023 DSR/X Motorcycles Due to Motor Controller Defect
Zero Motorcycles is recalling 2023 DSR/X motorcycles because incorrect fasteners in the motor controller may cause a loss of drive power, increasing crash risk.
Product
ZERO — ZERO DSR/X
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V828000·2025-12-01
Ford Recalls 2025 Maverick for Cylinder Head Manufacturing Defect
Ford is recalling 2025 Maverick vehicles with defectively manufactured cylinder heads that can leak oil. The leak increases the risk of fire and engine failure.
Product
FORD — FORD, LINCOLN EXPLORER, MUSTANG, MAVERICK, CORSAIR
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V827000·2025-12-01
Ford Recalls 2016-2019 Lincoln MKT for Detaching B-Pillar Trim
Ford is recalling 2016-2019 Lincoln MKT vehicles because the B-pillar door trim may detach while driving, creating a road hazard and increasing crash risk.
Product
LINCOLN — LINCOLN MKT
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V824000·2025-12-01
2019 Ram Trucks Recalled for Side Curtain Air Bag Inflator Defect
Chrysler is recalling 2019 Ram 1500, 2500, and 3500 vehicles because side curtain air bag inflators may rupture, potentially sending metal fragments into the cabin.
Product
RAM — RAM 1500, 2500, 3500
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V832000·2025-12-01
Virnig Recalls 2025 Trailers Due to Bearing Lock Nut Failure Risk
Virnig is recalling 2025 TR-HDD-1414 and TR-RHDD-1409 trailers because improperly installed bearing lock nuts may fail, causing the tire to detach and increasing crash risk.
Product
VIRNIG — VIRNIG TR-RHDD-1409, TR-HDD-1414
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V826000·2025-12-01
2025-2026 RAM Pickup Trucks: Blank Instrument Panel Display Software Error
Chrysler is recalling 2025-2026 RAM pickup trucks (1500, 2500, 3500, 4500, 5500) because a software error causes the instrument panel display to go blank, preventing drivers from seeing critical warning lights and gear selection.
Product
RAM — RAM 1500, 2500, 3500, 4500
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V825000·2025-12-01
KTM and Husqvarna motorcycles recalled for engine control software stalling defect
KTM and Husqvarna are recalling certain 2024-2025 motorcycles because faulty engine control software may cause the engine to stall at low RPMs, creating a risk of crashes.
Product
KTM — KTM, HUSQVARNA 390 SMC R, 390 ENDURO R, 390 ADVENTURE X, VITPILEN 401
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V833000·2025-12-01
Genesis G90 Models: Highway Drive Assist Braking Malfunction Recall
Hyundai is recalling 2023-2026 Genesis G90 vehicles because the Highway Drive Assist radar may falsely detect another vehicle, causing sudden braking that increases crash risk.
Product
GENESIS — GENESIS G90
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V829000·2025-12-01
2025 Ford Escape liftgate hinge covers may detach, creating crash risk
Ford is recalling certain 2025 Escape vehicles because liftgate hinge covers may not be properly secured and can detach. Detached covers can create a distraction or road hazard, increasing crash risk.
Product
FORD — FORD ESCAPE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V831000·2025-12-01
2025 Lincoln Navigator Rear Lightbar Cracks May Disable Reverse Lights
Ford is recalling certain 2025 Lincoln Navigator vehicles. The rear lightbar may develop cracks allowing moisture accumulation, potentially disabling reverse lights and reducing visibility when backing up.
Product
LINCOLN — LINCOLN NAVIGATOR
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V823000·2025-12-01
2025 Ford Expedition and Other Models Recalled for Brake Booster Malfunction
Ford is recalling 679 2025 Expedition, Ranger, F-150, Bronco, and Navigator vehicles due to a potential Electronic Brake Booster malfunction that can cause loss of power brake assist, increasing crash risk.
Product
FORD — FORD, LINCOLN F-150, EXPEDITION, BRONCO, RANGER
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25V830000·2025-12-01
Mercedes-Benz Recalls 2024-2025 AMG EQE SUV for Pedestrian Warning Sound Defect
Mercedes-Benz is recalling 2024-2025 AMG EQE SUV 4MATIC vehicles because a software error may prevent the pedestrian warning sound from increasing in volume with speed.
Product
MERCEDES-BENZ — MERCEDES-BENZ AMG EQE SUV 4MATIC
Category
Vehicle
Distribution
Distributed nationwide