The Recall Desk

State

North Carolina product recalls

73,495 recalls have nationwide distribution and so reach North Carolina. 10,298 additional recalls listed North Carolina specifically in their distribution scope.

What the numbers show

Total
10,298
Critical
1,486
Severe
2,898
Most recent
2026-10-14

Of the 10,298 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 10,298 recalls whose distribution notice names North Carolina specifically. The 73,495 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

22626–22650 of 83793

  • SevereFDA (Food)·F-1360-2022·2022-07-06

    Snack Fresh Apples and Peanut Butter Fruit Trays Recalled for Salmonella Risk

    Stellex/CF Houston, LLC is recalling 134,554 cases of Snack Fresh Apples and Peanut Butter fruit trays (6.5 oz) due to potential Salmonella contamination. Code dates 5/14/21–6/4/22 were distributed across 20 U.S. states.

    Product
    Snack Fresh Apples and Peanut Butter Net Wt 6.5 oz. packed in clear plastic non-flexible package UPC 0 74641 00044 6 six count per case
    Category
    Food
    Distribution
    20 states
  • SevereFDA (Food)·F-1367-2022·2022-07-06

    Peanut Butter Chocolate Fudge Bites Recalled for Salmonella Contamination

    Fudgeamentals LLC is recalling PEANUT BUTTER CHOCOLATE FUDGE BITES nationwide due to Salmonella contamination in the peanut butter ingredient. The recall affects 189,096 units.

    Product
    PEANUT BUTTER CHOCOLATE FUDGE BITES (24-8 OZ) FUDGEAMENTALS
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1366-2022·2022-07-06

    Chocolate Variety Tray Recalled for Salmonella Contamination in Peanut Butter

    Fudgeamentals Variety Tray (16 oz) is being recalled nationwide due to Salmonella contamination in its peanut butter component. Consumers should not consume the product and should discard it.

    Product
    VARIETY TRAY (16 OZ) (C-CNC-PBC) FUDGEAMENTALS
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1368-2022·2022-07-06

    Fudgeamentals Peanut Butter Fudge Bites Recalled for Salmonella Contamination

    Fudgeamentals is recalling Peanut Butter Fudge Bites nationwide due to Salmonella contamination in the peanut butter ingredient. Consumers should not consume the affected product.

    Product
    PEANUT BUTTER FUDGE BITES (24-8 OZ) FUDGEAMENTALS
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1363-2022·2022-07-06

    FDA recalls Giant Apples, Pretzels & Celery with peanut butter for Salmonella risk

    Stellex/CF Houston is recalling Giant Apples, Pretzels & Celery with peanut butter trays due to potential Salmonella contamination. The recall affects 134,554 cases distributed across 20 states from May 2021 through June 2022.

    Product
    Giant Apples, Pretzels & Celery with peanut butter Net Wt. 4 oz. packed in clear non-flexible plastic package UPC 6 88267 55369 1
    Category
    Food
    Distribution
    20 states
  • SevereNHTSA·22V477000·2022-07-06

    Travel Trailer Brake System Wiring Defect in Forest River Aurora

    Forest River Aurora travel trailers (2021-2022) have a brake system defect where the breakaway switch may be incorrectly wired, preventing trailer brakes from activating. Dealers will provide free inspection and repairs.

    Product
    COACHMEN — COACHMEN, FOREST RIVER CATALINA, AURORA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1361-2022·2022-07-06

    Snack Fresh Apple & Cheese Bites with Crackers recalled for potential Salmonella contamination

    Snack Fresh Apple & Cheese Bites with Crackers are being recalled nationwide due to potential Salmonella contamination. Consumers should not consume the product.

    Product
    Snack Fresh Apple & Cheese Bites with Crackers Net Wt. 4 oz. packed in clear non-flexible plastic package UPC 0 74641 32841 0 six count per case
    Category
    Food
    Distribution
    20 states
  • SevereFDA (Food)·F-1371-2022·2022-07-06

    Fudgeamentals Tiger Butter Fudge Bar Recalled for Salmonella

    Fudgeamentals LLC is recalling Tiger Butter Fudge Bar (8 oz) nationwide due to Salmonella contamination in the peanut butter ingredient. Affected lot codes: 22059007, 22083006, 22089006, 22130394.

    Product
    Fudgeamentals TIGER BUTTER FUDGE BAR (8 OZ)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-1370-2022·2022-07-06

    Fudge Trio Holiday Fudge Tray Recalled Nationwide for Salmonella Contamination

    Fudgeamentals LLC is recalling Marketside and Walmart Fudge Trio Holiday Fudge Trays nationwide due to Salmonella contamination in the peanut butter ingredient. Consumers should discard these products and not consume them.

    Product
    1. Marketside FUDGE TRIO HOLIDAY FUDGE TRAY - 16 oz. 2. WALMART MKT FUDGE TRIO (6-16 OZ) HOLIDAY FUDGE TRAY FUDGEAMENTALS
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·22V464000·2022-07-06

    Cummins Recalls 2020-2022 Trailer-Mounted Generator Sets Due to Shutdown Defect

    Cummins is recalling 2020-2022 C500D6Re trailer-mounted generator sets because a logic error may prevent them from shutting down, posing burn and shock risks.

    Product
    CUMMINS POWER GENERATION — CUMMINS POWER GENERATION GENERATOR SET
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1298-2022·2022-07-06

    TEG5000 Analyzer displays incorrect PlateletMapping assay results in TEG Manager

    Haemonetics' TEG5000 Analyzer displays incorrect PlateletMapping assay values when connected to TEG Manager Software versions 1.1–4.3.1, potentially affecting laboratory test interpretation.

    Product
    Product Name: TEG5000 Analyzer (07-022, 07-033) with TEG Analytical Software (07-030, 07-031) and TEG Platelet Mapping Assay - PlateletMapping ADP & AA (07-014), PlateletMapping ADP (07-015), PlateletMapping AA (07-016). Issue occurs when Platelet Mapping Assay results…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1172-2022·2022-07-06

    Fluticasone Propionate Nasal Spray Recalled Due to Defective Container

    Akorn, Inc. is recalling 44,400 bottles of Fluticasone Propionate Nasal Spray nationwide due to a defective container that prevents proper dispensing. Patients should contact their healthcare provider or pharmacist.

    Product
    Fluticasone Propionate Nasal Spray, USP, 50 mcg, 16 g net fill weight per amber glass bottle, Rx only, Manufactured by: HI-TECH PHARMACAL CO., INC., Amityville, NY 11701. NDC 50383-700-16
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1385-2022·2022-07-06

    Wilton Rainbow Chip Crunch Sprinkles recalled due to milk contamination

    Wilton Industries is recalling Rainbow Chip Crunch Sprinkles (5.25 oz) due to milk contamination. The recall affects 6,400 units distributed nationwide and internationally.

    Product
    Wilton Rainbow Chip Crunch Sprinkles net wt 5.25 oz. item 710-5364
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1300-2022·2022-07-06

    Orthopedic Plates Recalled Due to Incorrect Etching and Mislabeling

    One lot of DVR Anatomic distal radius orthopedic plates was incorrectly etched during manufacturing and may have been placed into kits labeled as a different plate model. The affected plates were distributed to healthcare facilities nationwide.

    Product
    DVR Anatomic, Model No. DVRAR. Distal Volar Radius Anatomical Plate System used for the fixation of fractures and osteotomies involving the distal radius.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22E054000·2022-07-06

    Cummins Recalls PD7000 Electric Drivetrains Due to Electrical Grounding Defect

    Cummins is recalling PD7000 Electric Drivetrains because an improperly grounded air compressor can cause electric shock. Owners will receive a free repair to install a ground strap.

    Product
    ELECTRICAL SYSTEM:PROPULSION SYSTEM recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1285-2022·2022-07-06

    Backup batteries in Avance CS2 anesthesia machines fail prematurely

    GE Healthcare is recalling backup batteries in Avance CS2 and CS2 Pro anesthesia machines manufactured after April 1, 2019. Batteries may fail earlier than expected, affecting approximately 6,600 devices worldwide.

    Product
    Back up batteries in Avance CS2 and Avance CS2 Pro anesthesia devices manufactured on or after April 1, 2019
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1309-2022·2022-07-06

    GCX Channel Mounting Accessory Screws May Loosen or Pull Out

    Skytron recalls its GCX Channel Mounting Accessory (model H8-300-40-A) because mounting screws may loosen or pull out when used as a monitor mount on surgical booms. Affected units were distributed worldwide.

    Product
    Product Name: GCX Channel Mounting Accessory Model/Catalog Number: H8-300-40-A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1169-2022·2022-07-06

    Methylphenidate Patch Recall: Defective Delivery System and Adhesive Issues

    Daytrana (methylphenidate) patches are being recalled due to ripping patches and poor adhesive transfer affecting drug delivery. This Class II recall involves 8,559 cartons distributed nationwide.

    Product
    DAYTRANA — DAYTRANA (METHYLPHENIDATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1162-2022·2022-07-06

    Losartan Potassium tablets recalled for elevated AZIDO impurity

    PD-Rx Pharmaceuticals recalled Losartan Potassium 50 mg tablets nationwide due to AZIDO impurity levels exceeding acceptable manufacturing limits. The recall affects 687 bottles across multiple lots.

    Product
    LOSARTAN POTASSIUM — LOSARTAN POTASSIUM (LOSARTAN POTASSIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1304-2022·2022-07-06

    HydroSurg Plus Laparoscopic Irrigator recalled for inability to irrigate

    Davol HydroSurg Plus Laparoscopic Irrigators cannot provide irrigation. The FDA issued a Class II recall affecting 4,780 units worldwide.

    Product
    HydroSurg Plus Laparoscopic Irrigator with Nezhat-Dorsey SmokEvac Trumpet Valve, Handle only, with Cojoined Suction and Irrigation Tubing, Catalog number 0026880
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1295-2022·2022-07-06

    CV Minor Kit with Nonsterile Component Recalled for Contamination Risk

    ROi CPS LLC is recalling 180 CV Minor Kit units due to a nonsterile component accidentally packaged in the sterile kit, posing a contamination and infection risk.

    Product
    regard Item Number: 800774001, CV00979A - CV Minor Kit, Sterile.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1292-2022·2022-07-06

    Medical Device App Records Inaccurate Urinary Flow When Hearing Aids Active

    The ProudP Everyday Uroflow Tracker app may record lower-than-actual urination measurements when a hearing aid or AirPods Live Listen feature is active on the same iPhone, due to interference with the app's sound-based measurement system.

    Product
    ProudP Everyday Uroflow Tracker Software Version 1.x.x Software Version 1.2.0 or earlier
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1290-2022·2022-07-06

    Central venous catheter recalled for incorrect gravity flow rates

    Arrow International is recalling the Arrow Three-Lumen CVC due to incorrect gravity flow rates on the product lidstock. The defect may affect fluid and medication delivery through the catheter.

    Product
    Arrow Three-Lumen CVC
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1161-2022·2022-07-06

    Losartan Potassium Tablets Recalled for Manufacturing Impurity Issues

    PD-Rx Pharmaceuticals recalls Losartan Potassium Tablets (25 mg, 90-tablet bottles) due to Current Good Manufacturing Practice deviations. Specific lot numbers contain AZIDO impurity levels above acceptable limits.

    Product
    LOSARTAN POTASSIUM — LOSARTAN POTASSIUM (LOSARTAN POTASSIUM)
    Category
    Drug
    Distribution
    Distributed nationwide