The Recall Desk

State

North Carolina product recalls

73,092 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 73,092 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

9201–9225 of 83386

  • HighFDA (Devices)·Z-0626-2025·2024-12-11

    Medline recalls surgical convenience kits with defective smoke evacuation component

    Medline is recalling five types of medical convenience kits because they contain the SafeAir Smoke Evacuation Pencil, which Stryker subsequently recalled.

    Product
    MEDLINE convenience kits labeled as: 1) CVL PACK, REF DYNJ00281O; 2) VASCULAR ACCESS PACK-LF, REF DYNJ0101291F; 3) MAJOR VASCULAR PACK-LF, REF DYNJ0488546K; 4) PEDS CENTRAL LINE PACK, REF DYNJ84762; 5) PACK,CENTRAL LINE, REF DYNJ906907C
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0081-2025·2024-12-11

    Iron sucrose injection recall due to potential glass contamination in vials

    VENOFER (iron sucrose) injection is being recalled nationwide because certain vials may contain glass particles from potential glass delamination. Patients and healthcare providers should contact their pharmacist or healthcare provider immediately.

    Product
    VENOFER — VENOFER (IRON SUCROSE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·24V923000·2024-12-11

    Suzuki Recalls 2023-2025 Burgman 400 Scooters for Fuel Leak Risk

    Suzuki is recalling 2023-2025 Burgman 400 scooters because a fuel supply hose may contact a vapor hose, causing fuel leaks that increase fire risk.

    Product
    SUZUKI — SUZUKI AN400
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0225-2025·2024-12-11

    Gordon CHOICE Fruit Punch Mix Recalled for Metal Fragment Contamination

    Gordon CHOICE Fruit Punch Mix is being recalled due to metal fragments introduced during production. The affected product was distributed to 29 states.

    Product
    Gordon CHOICE Fruit Punch Beverage Mix Naturally and Artificially Flavored Low Calorie Instant, NET WT. 8.6 OZ (243 g), UPC 0 93901 59606 2, Case UPC 10093901596069 & NET WT. 22OZ (1 LB 6 OZ) 624 g, 0 93901 28673 4, Case UPC 10093901286731, FOR DISTRIBUTION EXCLUSIVELY BY PARA SU
    Category
    Food
    Distribution
    30 states
  • HighNHTSA·24V921000·2024-12-11

    Gillig Recalls 2023 Low Floor Buses Due to Odometer Defect

    Gillig is recalling 2023 Low Floor diesel-hybrid transit buses because the odometer fails to display mileage in electric mode, potentially delaying critical maintenance.

    Product
    GILLIG — GILLIG LOW FLOOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0586-2025·2024-12-11

    Medical Device Data Management Software Affected by Unauthorized Service Credential Access

    Service credentials for BD EpiCenter Data Management System were accessed by an unauthorized actor. This creates a risk of unauthorized access to the software and associated data until credentials are updated.

    Product
    BD EpiCenter Data Management System, Multi User Software Version or Model: 440981 Catalog Number: 440981
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0596-2025·2024-12-11

    Medical Device Breach: BACTEC 9240 System Faces Unauthorized Access Risk

    Becton Dickinson recalled the BACTEC 9240 System after unauthorized actors accessed product service credentials. Until credentials are updated, there is risk of unauthorized access that may compromise system security and data integrity.

    Product
    BACTEC 9240 System Version or Model: 445475 Catalog Number: 445475
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0242-2025·2024-12-11

    Chocolate Pudding Mix Recalled for Metal Fragment Contamination

    Monarch Instant Chocolate Pudding & Pie Filling Mix is being recalled due to metal fragments introduced during production. The affected product was distributed to 29 states.

    Product
    MONARCH INSTANT CHOCOLATE PUDDING & PIE FILLING MIX NATURALLY AND ARTIFICIALLY FLAVORED, NET WT. 24OZ, Case UPC 50758108068983 DISTRIBUTED BY US FOODSS, INC ROSEMONT, IL 60018
    Category
    Food
    Distribution
    30 states
  • HighFDA (Devices)·Z-0632-2025·2024-12-11

    MEDLINE Port Insertion Pack Recalled for Defective Component

    Medline is recalling 44 PORT INSERTION PACK kits nationwide. These kits contain SafeAir Smoke Evacuation Pencil components that were previously recalled by Stryker.

    Product
    MEDLINE convenience kits labeled as: PORT INSERTION PACK, REF DYNJ81597
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0106-2025·2024-12-11

    Duloxetine Delayed-Release Capsules Recalled for N-Nitroso Impurity Above Limits

    Rising Pharma is recalling 122,925 bottles of Duloxetine 30 mg capsules nationwide due to a manufacturing deviation: the presence of N-nitroso-duloxetine impurity above the recommended interim limit.

    Product
    Duloxetine Delayed-Release Capsules USP, 30 mg, a) 30 count (NDC 57237-018-30), b) 90 count (NDC 57237-018-90) and c) 1000 count (NDC 57237-018-99) bottles, Rx only, Distributed by: Rising Pharma Holdings, Inc., East Brunswick, NJ
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0621-2025·2024-12-11

    BD Bacterial Susceptibility Test Discs Recall for Decreased Potency

    Becton Dickinson recalled BD BBL Sensi Disc Ampicillin 2 μg test discs due to 65% potency loss over 18 months that may produce false resistant results in susceptibility testing.

    Product
    BD BBL Sensi Disc Ampicillin 2 ¿g (AM-2) - In-Vitro BD BBL Sensi Disc Ampicillin 2 ¿g (AM-2) are used for semi-quantitative in vitro susceptibility testing by the agar disc diffusion test procedure of common, rapidly growing and certain fastidious bacterial pathogens. Catalog
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0107-2025·2024-12-11

    Duloxetine DR Capsules recalled nationwide for nitrosamine impurity

    Rising Pharmaceuticals is recalling Duloxetine DR Capsules 60 mg nationwide due to N-nitroso-duloxetine impurity levels exceeding FDA interim limits. The recall affects approximately 233,003 bottles.

    Product
    Duloxetine DR Capsules USP 60 mg, a) 30 count (NDC 57237-019-30), b) 90 count NDC 57237-019-90 and c) 1000 count (NDC 57237-019-99) bottles, Distributed by: Rising Pharmaceuticals, Inc., East Brunswick, NJ
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0090-2025·2024-12-11

    ROYALAB Germ Away Antibacterial Hand Soap Recalled for Failed Microbiological Testing

    Midlab Incorporated is recalling ROYALAB Germ Away Antibacterial Hand Soap (1-gallon, Lot 0711241) due to out-of-specification microbiological test results. The product failed manufacturing quality standards.

    Product
    ROYALAB Germ Away Antibacterial Hand Soap, Chloroxylenol 0.1%, NET CONTENTS: ONE U.S. GALLON (3.78 L), Royal Papers, 2701 Hereford St., St. Louis, MO 63139
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0223-2025·2024-12-11

    Vanilla Instant Pudding Mix Recalled for Contamination with Metal Fragments

    DYMA Brands is recalling Culinary Secrest Originals Vanilla Instant Pudding Mix because a damaged sifter introduced metal fragments into the product. Consumers should not consume the product.

    Product
    CULINARY SECREST ORIGINALS VANILLA INSTANT PUDDING MIX NATURAL & ARTIFICIAL FLAVOR, NET WT. 24 OZ. (1.5 LB.) 680g, 8 UPC 22486 19071 2, Case UPC 30822486190706 and NET WT. 28 OZ. (1.75 LB.) 793g, UPC 8 22486 19070 5, Case UPC 30822486190706, MARKETED BY INDEPENDENT MARKETING ALLI
    Category
    Food
    Distribution
    30 states
  • HighFDA (Food)·F-0233-2025·2024-12-11

    Sysco Pink Lemonade Drink Mix Recalled for Metal Fragment Contamination

    Sysco Classic Pink Lemonade Drink Mix is recalled because a damaged sifter during production introduced metal fragments into the product. Products were distributed across 29 states.

    Product
    Sysco Classic Pink Lemonade Drink Mix Natural Flavor, NET WT. 24OZ(1 LB 8 OZ) 680 g, UPC 0 74865 09326 2, Case UPC 10074865093269, DISTRIBUTED BY SYSCO CORPORATION, HOUSTON, TEXAS 77077
    Category
    Food
    Distribution
    30 states
  • HighFDA (Drugs)·D-0079-2025·2024-12-11

    Cinacalcet Tablets Recalled for N-Nitroso Impurity Exceeding FDA Safety Limit

    Aurobindo Pharma USA recalls Cinacalcet 90 mg tablets nationwide due to N-nitroso impurity exceeding FDA's interim safety limit. The impurity is a known carcinogenic compound.

    Product
    Cinacalcet Tablets, 90 mg, packaged in: a) 30-count HDPE bottle (NDC 65862-833-30), b) 500-count HDPE bottle (NDC 65862-833-05), Rx Only, Distributed by: Aurobindo Pharma USA, Inc. 279 Princeton-Hightstown Road, East Windsor, NJ 08520, Made in India. 90 mg - 30 Tablets - NDC 658
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0241-2025·2024-12-11

    Thirster Low Cal Fruit Recalled for Metal Fragment Contamination

    Dyma Brands recalls Thirster Low Cal Fruit due to metal fragments in the product from a damaged sifter during dextrose production. The affected pouches were distributed across 29 states.

    Product
    THIRSTER LOW CAL FRUIT, NET WT. 8.6OZ, Case UPC 50758108397380, DISTRIBUTED BY US FOODS, INC. ROSEMONT, IL 60018
    Category
    Food
    Distribution
    30 states
  • HighFDA (Food)·F-0251-2025·2024-12-11

    Apple Wedge Apple Cider Recalled for Elevated Patulin Levels

    Apple Wedge 100% Pasteurized Apple Cider with code C3419 was recalled for containing patulin at 78 ppb, exceeding the FDA limit of 50 ppb. Products were distributed to GA, NC, SC, and FL.

    Product
    No Preservatives 100% CIDER Pasteurized APPLE WEDGE CIDER 1/2 Gal. (1.89L) HENDERSONVILLE, NC 28792 Keep Refrigerated Produce of USA UPC 0 36482 64000 7
    Category
    Food
    Distribution
    4 states
  • HighFDA (Devices)·Z-0585-2025·2024-12-11

    BD EpiCenter Data Management System Credential Compromise Poses Unauthorized Access Risk

    Service credentials for the BD EpiCenter Data Management System were accessed by an unauthorized actor. Until credentials are updated, system data and access controls are at risk.

    Product
    BD EpiCenter Data Management System Version or Model: 440887 Catalog Number: 440887
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0231-2025·2024-12-11

    Sysco Fruit Punch Drink Mix recalled for metal fragments

    Sysco Classic Fruit Punch Drink Mix is being recalled due to metal fragments introduced by a damaged sifter during manufacturing. The affected product (Case UPC 00734730132709, Lot 263 EFA) was distributed across 29 states.

    Product
    Sysco Classic Fruit Punch Drink Mix Natural and Artificial Flavor, NET WT. 8.6OZ (244 G), Case UPC 00734730132709, DISTRIBUTED BY SYSCO CORPORATION, HOUSTON, TEXAS 77077
    Category
    Food
    Distribution
    30 states
  • ModerateFDA (Devices)·Z-0588-2025·2024-12-11

    BD COR MX Instruments Affected by Unauthorized Service Credentials Access

    BD recalled its COR MX instruments after an unauthorized actor accessed service credentials. The company is updating credentials to prevent future unauthorized access to product data and systems.

    Product
    BD COR MX Instrument Version or Model: 443989 Catalog Number: 443989
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0594-2025·2024-12-11

    BD BACTEC FX40 Product Service Credentials Accessed by Unauthorized Actor

    Unauthorized actor accessed BD technical support credentials for the BACTEC FX40 laboratory instrument. Until credentials are updated, there is a risk of unauthorized access to the system and associated data.

    Product
    BD BACTEC FX40 Instrument Version or Model: 442296 Catalog Number: 442296
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0623-2025·2024-12-11

    Medline Medical Convenience Kits Recall Due to Recalled Component

    Medline is recalling certain medical convenience kits manufactured with SafeAir Smoke Evacuation Pencils that were previously recalled by Stryker. The recall affects 182 units distributed nationwide.

    Product
    MEDLINE medical convenience kits labeled as: 1) ACETABULAR PACK-LF, REF DYNJ0572894I; 2) LOCAL BASIC, REF DYNJ34418L; 3) LOCAL BASIC, REF DYNJ34418M; 4) MINI LOCAL, REF DYNJ900287D
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0642-2025·2024-12-11

    Medline Surgical Convenience Kits Recalled Over Supplier Component Recall

    Medline is recalling 336 surgical convenience kits manufactured with SafeAir Smoke Evacuation Pencils that Stryker previously recalled. The kits were distributed nationwide.

    Product
    MEDLINE convenience kits labeled as: 1) LITHOTOMY/PELVISCOPY PACK, REF DYNJ0531985R; 2) PELVISCOPY PACK-LF, REF DYNJ0843760I; 3) PELVISCOPY PACK-LF, REF DYNJ0843760J
    Category
    Medical Device
    Distribution
    Distributed nationwide