The Recall Desk

State

North Carolina product recalls

72,992 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.

These figures cover only the 10,261 recalls whose distribution notice names North Carolina specifically. The 72,992 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

8201–8225 of 83253

  • SevereFDA (Drugs)·D-0223-2025·2025-02-12

    Adrenalin Chloride Epinephrine Nasal Solution Recalled for Misleading Label

    Par Pharmaceutical is recalling Adrenalin Chloride Solution (Epinephrine Nasal Solution) due to a misleading label that resembles the FDA-approved Adrenalin epinephrine injection product, creating potential confusion.

    Product
    Adrenalin Chloride Solution (Epinephrine Nasal Solution, USP), 30mg/30mL (1mg/mL), packaged in 30 mL vials, Distributed by: Par Pharmaceutical, Chestnut Ridge, NY 10977, NDC 42023-103-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0533-2025·2025-02-12

    Seasoned Bread Crumbs Recalled Due to Undeclared Sesame Allergen

    La Fiesta Food Products is recalling seasoned bread crumbs because they contain undeclared sesame, an allergen not listed on the label. The product was distributed nationwide.

    Product
    La Fiesta PAN RAYADO SAZONADO Bread Crumbs Seasoned, NET WT 8 OZ. (227g), UPC# 032327000887
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0532-2025·2025-02-12

    La Fiesta Bread Crumbs Recalled for Undeclared Sesame Allergen

    La Fiesta PAN RAYADO Bread Crumbs are being recalled for undeclared sesame, an allergen not listed on the label. The recall affects 2,200 cases distributed nationwide.

    Product
    La Fiesta PAN RAYADO Bread Crumbs, NET WT 8 OZ. (227g), UPC# 032327000886
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0467-2025·2025-02-12

    Atkinson's Plain Hushpuppies Recalled Due to Undeclared Milk Allergen

    Atkinson Milling Company is recalling Atkinson's No Onions Plain Hushpuppies due to undeclared milk on the label. Consumers with milk allergies who consume this product risk allergic reaction.

    Product
    ATKINSON'S NO ONIONS PLAIN NO ONIONS HUSHPUPPIES NET WT. 2 LB. 8 OZ. UPC 0 72119 20304 7 Ingredients: Enriched Whole Grain Corn Meal***Enriched Wheat Flour, Sugar, Onions, Salt, Eggs, Sodium Bicarbonate Sodium Aluminum Phosphate, Acidic Monocalcium Phosphate and Natural Flavors.
    Category
    Food
    Distribution
    8 states
  • SevereFDA (Food)·F-0461-2025·2025-02-12

    NuGo Dark Chocolate Pretzel Bars Recalled for Undeclared Milk Allergen

    Bazzini LLC is recalling NuGo Dark Chocolate Pretzel bars because they contain undeclared milk. Consumers with milk allergies should not consume the affected product.

    Product
    NuGo Dark Chocolate Pretzel with Sea Salt , Real Dark Chocolate / Vegan. 12g Protein
    Category
    Food
    Distribution
    13 states
  • SevereFDA (Food)·F-0463-2025·2025-02-12

    NuGo Dark Pretzel Chocolate Chip Bars Recalled for Undeclared Milk

    Bazzini LLC is recalling NuGo Dark Pretzel/Chocolate Chip Multipack bars due to undeclared milk. The product poses a risk to consumers with milk allergies.

    Product
    NuGo Dark Pretzel/Chocolate Chip Multipack 18 ct., 50g bar, 18 bars/tray, 9 trays/case. 40case/pallet
    Category
    Food
    Distribution
    13 states
  • SevereFDA (Food)·F-0462-2025·2025-02-12

    NuGo Dark Chocolate Chip Bars Recalled for Undeclared Milk

    Bazzini LLC is recalling NuGo Dark Chocolate Chip bars because they contain undeclared milk, which poses a health risk to consumers with milk allergies.

    Product
    NuGo Dark Chocolate Chip, Real Dark Chocolate / Vegan. 12g Protein
    Category
    Food
    Distribution
    13 states
  • SevereFDA (Food)·F-0466-2025·2025-02-12

    Atkinson's Hushpuppies Recalled Due to Undeclared Milk Allergen

    Atkinson Milling Company is recalling Atkinson's Hushpuppies with Onions due to undeclared milk. The product was not labeled as containing milk, posing a risk to consumers with milk allergies.

    Product
    ATKINSON'S HUSHPUPPIES WITH ONIONS NET WT. 1LB. (454 g) UPC 0 72119 20718 2 and NET WT. 2 LB. 8 OZ. UPC 0 72119 20305 4 Ingredients: Enriched Whole Grain Corn Meal***Enriched Wheat Flour, Sugar, Onions, Salt, Eggs, Sodium Bicarbonate Sodium Aluminum Phosphate, Acidic Monocalcium
    Category
    Food
    Distribution
    8 states
  • SevereNHTSA·25V077000·2025-02-12

    Terberg Benschop Recalls 2023-2024 YT Series Vehicles for Steering Defect

    Terberg Benschop is recalling 2023-2024 YT Series vehicles because a steering arm bolt may be improperly tightened, risking loss of steering and a crash.

    Product
    TERBERG BENSCHOP B.V. — TERBERG BENSCHOP B.V. YT SERIES
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·005-2025·2025-02-12

    Common Sense Soap Recalls Uninspected Beef Tallow Products

    Common Sense Soap is recalling approximately 33,899 pounds of beef tallow products produced without federal inspection. The products were shipped nationwide and lack a USDA mark of inspection.

    Product
    Common Sense Soap Recalls Beef Tallow Products Produced Without Benefit of Inspection
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·25V080000·2025-02-12

    Audi Q5 and A7 high voltage batteries may overheat

    Volkswagen is recalling certain 2021-2024 Audi Q5 and 2022 A7 e plug-in hybrid vehicles because the high-voltage battery may overheat, increasing the risk of a fire.

    Product
    AUDI — AUDI Q5, A7 E
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V079000·2025-02-12

    Porsche Recalls 2025 911 Models Due to Headlight Glare Software Error

    Porsche is recalling 878 2025 911 vehicles because a software error causes low beam headlights to create excessive glare for oncoming traffic, increasing crash risk.

    Product
    PORSCHE — PORSCHE 911
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0516-2025·2025-02-12

    Apple Cider Cake Rings Recalled for Potential Listeria Contamination

    FGF, LLC is recalling Just Baked Apple Cider Cake Rings due to potential Listeria monocytogenes contamination. Approximately 2,017,614 cases were distributed nationwide in the US and Canada.

    Product
    item 8201901 JUST BAKED APPLE CIDER CAKE RINGS WITH NATURAL FLAVORS 144x2.5OZ, NET WT 22.5 LB
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0521-2025·2025-02-12

    FDA Recalls Apple Crisp Cake Donuts for Potential Listeria Contamination

    FGF, LLC recalls Apple Crisp Cake Donuts for potential Listeria monocytogenes contamination. Approximately 2,017,614 cases are affected.

    Product
    item 8201920 APPLE CRISP CK DONUT PFD 78x3OZ, NET WT 13.16 LB
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1115-2025·2025-02-12

    Beckman Coulter DxI 9000 immunoassay analyzer recalled for software-related motion errors

    Beckman Coulter is recalling 61 DxI 9000 immunoassay analyzers worldwide due to a software error causing tray gripper motion errors that result in intermittent hard stops and delays in patient test results.

    Product
    Beckman Coulter DxI 9000 Access Immunoassay Analyzer, catalog number C11137; in-vitro diagnostic instrument
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0496-2025·2025-02-12

    Frozen donuts recalled for potential listeria monocytogenes contamination

    FGF, LLC is recalling frozen donuts nationwide due to potential contamination with listeria monocytogenes. Consumers should not consume the product and should discard or return it.

    Product
    item 8201848 GEN HEX RG DONUT DGH FRZ 96x2.75OZ, NET WT 14.86 LB
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1113-2025·2025-02-12

    Sysmex PS-10 Sample Preparation System Recalled for False Test Results

    Sysmex PS-10 Sample Preparation Systems may produce false test results due to sporadic omission of the probe wash step during antibody pipetting. Thirty-two units have been recalled nationwide.

    Product
    Sysmex PS-10 Sample Preparation System with software version 1.5 and 1.6., Catalog Number BQ716341. Product usage for automated pipetting, diluting, and specimen processing workstations for flow cytometric analysis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1107-2025·2025-02-12

    Patient Monitor May Fail to Alarm on Ventilator Disconnect

    Philips IntelliVue Patient Monitor MX400 may fail to alarm when a Hamilton ventilator is disconnected. 28 units affected in the US and internationally.

    Product
    IntelliVue Patient Monitor MX400. Model Number: 866060
    Category
    Medical Device
    Distribution
    2 states
  • HighFDA (Food)·F-0528-2025·2025-02-12

    Unfilled Bismarck Donuts Recalled Due to Listeria Contamination Risk

    FGF, LLC is recalling over 2 million cases of unfilled Bismarck donuts due to potential Listeria monocytogenes contamination. The recall affects products distributed nationwide in the US and Canada.

    Product
    item 8202731 UNFLD BISMARK DONUT PFD 78X3OZ, NET WT 13.16 LB
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0506-2025·2025-02-12

    FGF Fluff Donuts Recalled for Potential Listeria Contamination

    FGF, LLC is recalling 2,017,614 cases of item 8201870 Fluff Donuts due to potential Listeria monocytogenes contamination. The affected product was produced on or before December 13, 2024, and distributed nationwide in the US and Canada.

    Product
    item 8201870 GEN BAR FLUFF DONUT ZGT PFD 78x3OZ, NET WT 13.16 LB
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0512-2025·2025-02-12

    FGF LLC Recalls Unfilled Bismarck Donuts for Listeria Contamination Risk

    FGF LLC is recalling 2,017,614 cases of unfilled Bismarck donuts nationwide due to potential listeria monocytogenes contamination. Consumers should not consume the affected product.

    Product
    item 8201883 UNFLD BISMARK DONUT PFD 57x2.75OZ, NET WT 8.82 LB
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1091-2025·2025-02-12

    Philips Azurion and Allura System Patient Tables: Finger Entrapment Risk

    Philips Azurion and Allura system patient tables may trap fingers between the guiding rails and tabletop during manual repositioning, risking finger injury to operators and service personnel.

    Product
    Azurion 7 B12 System Code: (1) 722067 (2) 722225 (3) 722235
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1093-2025·2025-02-12

    Philips Azurion patient tables recalled for finger entrapment risk

    Philips is recalling Azurion 7 M12 and Allura patient tables used in medical imaging systems due to a finger entrapment hazard during manual repositioning. Operators and service personnel may suffer finger injury if fingers are caught between the tabletop and guiding rails.

    Product
    Azurion 7 M12 System Code: (1) 722078 (2) 722223 (3) 722233
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1080-2025·2025-02-12

    Philips recalls AlluraXper FD20 patient tables due to finger entrapment hazard

    Philips is recalling AlluraXper FD20 patient tables due to a finger entrapment hazard. During manual repositioning, fingers can get trapped between the tabletop and rails, risking injury to operators and service personnel.

    Product
    AlluraXper FD20 System Code: (1) 722006 (2) 722012 (3) 722028
    Category
    Medical Device
    Distribution
    Distributed nationwide