The Recall Desk

State

North Carolina product recalls

73,219 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 73,219 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

15601–15625 of 83513

  • ModerateFDA (Food)·F-1531-2023·2023-09-27

    Pasteurized Cheese Product Recalled for Inconsistent Refrigeration Instructions on Labels

    Great Lakes Cheese, Inc. is recalling Hill Country Fare Melt'n Cheese because product labels contain inconsistent refrigeration requirements, which may result in improper storage by consumers.

    Product
    Hill Country Fare Melt'n Cheese, Pasteurized Prepared Cheese Product, Net Wt 32 oz (2 lbs) 907g. UPC 0 41220-77273 5. Refrigerate after Opening. Distributed By: H-E-B, San Antonio, TX 78204
    Category
    Food
    Distribution
    32 states
  • ModerateFDA (Devices)·Z-2627-2023·2023-09-27

    Epidural Anesthesia Sets Recalled Due to Incorrect Lid Stock Label

    B. Braun Medical is recalling approximately 3,440 Perifix® epidural anesthesia sets due to incorrect labeling of the lid stock. The mislabeled products were distributed to multiple U.S. states.

    Product
    Perifix¿ / Epidural anesthesia set, medicated
    Category
    Medical Device
    Distribution
    13 states
  • ModerateFDA (Food)·F-1533-2023·2023-09-27

    HEB Easy Melt Salsa Queso Recalled Due to Conflicting Refrigeration Labels

    HEB Easy Melt Salsa Queso is recalled for conflicting refrigeration labels that may cause improper storage. Over 7.2 million pounds were distributed across 32 states.

    Product
    HEB Easy Melt Salsa Queso, with Tomatoes, Jalapeno Peppers & Onions, Net Wt 32 oz (2 lbs) 907g. UPC 0 41220-33063 8. Refrigerate after Opening. Made with Pride and Care for H-E-B, San Antonio, Texas 78204
    Category
    Food
    Distribution
    32 states
  • ModerateFDA (Devices)·Z-2613-2023·2023-09-27

    Prucka 3 Amplifier Power Supply May Fail and Cause Device Inoperability

    GE Medical Systems is recalling Prucka 3 Amplifiers and related field replaceable units used in CardioLab and ComboLab systems. A power supply diode may overheat and fail, causing the amplifier to stop working.

    Product
    Prucka 3 Amplifiers, Model P1801PA, and Field Replaceable Units (FRUs), Model 5875569, used with CardioLab AltiX and ComboLab AltiX.
    Category
    Medical Device
    Distribution
    17 states
  • ModerateFDA (Food)·F-1528-2023·2023-09-27

    Refrigerated Pasteurized Cheese Products Recalled Due to Labeling Inconsistency

    Great Value and SE Grocers refrigerated cheese products are being recalled because labels contain inconsistent refrigeration requirements, which may result in improper storage by consumers.

    Product
    Pasteurized Prepared Cheese Product packaged under the following brands and sizes: 1. Great Value Original Melt'n Dip Easy Melt Cheese, Net Wt 16 oz (1 lb) 453g. UPC 0 78742-01512 5. Refrigerate after Opening. Distributed By: Walmart Inc., Bentonville, AR 72716 2.…
    Category
    Food
    Distribution
    32 states
  • ModerateFDA (Drugs)·D-1168-2023·2023-09-27

    ChloraPrep One-Step Topical Applicators Recalled for Unsupported Shelf-Life Claims

    BD ChloraPrep One-Step topical applicators are recalled because the 36-month shelf life is not supported by stability data; the product may develop fungal contamination beyond 12 months.

    Product
    CHLORAPREP ONE-STEP — CHLORAPREP ONE-STEP (CHLORHEXIDINE GLUCONATE AND ISOPROPYL ALCOHOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1529-2023·2023-09-27

    Harris Teeter Cheesy Melt recalled for labeling refrigeration requirements

    Harris Teeter Cheesy Melt pasteurized cheese product is recalled because labeling variations may prevent proper refrigeration. Approximately 7.2 million pounds are affected across 31 states with use-by dates of March 8, 2024 and earlier.

    Product
    Harris Tetter Cheesy Melt, Pasteurized Prepared Cheese Product, Net Wt 32 oz (2 lbs) 907g. UPC 0 72036-70682 9. After Opening, Refrigerate Up to 8 weeks. Do Not Freeze. Proudly Distributed By: Harris Teeter, LLC, Matthews, NC 28105
    Category
    Food
    Distribution
    32 states
  • ModerateFDA (Drugs)·D-1172-2023·2023-09-27

    Cequa cyclosporine ophthalmic solution recalled nationwide for subpotency

    Sun Pharmaceutical is recalling Cequa (cyclosporine) ophthalmic solution because certain lots contain less active ingredient than specified. Contact your doctor if using an affected product.

    Product
    CEQUA — CEQUA (CYCLOSPORINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1523-2023·2023-09-27

    Cheese Spread Products Recalled for Inconsistent Refrigeration Requirements

    Multiple cheese spread brands are being recalled due to inconsistent refrigeration instructions on labels. Consumers should verify proper storage and discard products with unclear label instructions.

    Product
    Cheese Spread Pasteurized Process packaged under the following brands and sizes: 1. bowl & Basket, A Shoprite Brand, Net Wt 32 oz (2lb)907g. UPC 0 41190-46935 2. Refrigerate after Opening. Distributed by: Wakeforn Food Corp, 5000 Riverside Drive, Keasbey, NJ 08832 2.…
    Category
    Food
    Distribution
    32 states
  • LowFDA (Devices)·Z-2591-2023·2023-09-27

    Arrow ErgoPack PICC catheter kits recalled for incorrect product labeling

    Arrow International recalled 177 ErgoPack PICC catheter kits because the product code and name were incorrectly listed on the packaging. No illnesses or injuries reported.

    Product
    Arrow ErgoPack, Pressure Injectable Two-Lumen PICC pre-loaded with Arrow VPS Stylet, REF CDC-35552-VPS; Catheter: Percutaneous, implanted, long-term intravascular catheter
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V652000·2023-09-25

    Kia Recalls Multiple Models Due to Electrical Short Fire Risk

    Kia is recalling 1.7 million vehicles because an electrical short in the brake control unit may cause an engine compartment fire.

    Product
    KIA — KIA SORENTO, RIO, OPTIMA HYBRID, SOUL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V651000·2023-09-22

    Hyundai Recalls Multiple Models Due to ABS Module Fire Risk

    Hyundai is recalling over 1.6 million vehicles because a leaking ABS module may cause an engine compartment fire. Owners should park outside until the repair is complete.

    Product
    HYUNDAI — HYUNDAI ELANTRA, AZERA, SANTA FE, GENESIS COUPE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V649000·2023-09-22

    2023 Kia Forte Right Front Control Arm Defect Recall

    Kia is recalling 2023 Forte vehicles due to improper welds on the right front lower control arm, which may fail and cause loss of steering control. Affected owners should not drive the vehicle until repaired.

    Product
    KIA — KIA FORTE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V648000·2023-09-22

    2024 East to West RV Recall: Detachable Rear Ladder Poses Injury Risk

    Forest River is recalling certain 2024 East to West Blackthorn and Tandara fifth wheels. The rear ladder may detach due to improper anchoring, creating a potential injury risk.

    Product
    EAST TO WEST — EAST TO WEST BLACKTHORN, TANDARA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V650000·2023-09-22

    2024 Hyundai Kona Seat Belt Retractor Malfunction Recall

    Hyundai is recalling certain 2024 Kona vehicles because the rear seat belt retractors may not function properly. A defective seat belt could fail to restrain occupants in a crash, increasing injury risk.

    Product
    HYUNDAI — HYUNDAI KONA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·23290·2023-09-21

    HONEY JOY Infant Swings Recalled for Suffocation Hazard

    HONEY JOY infant swings are recalled due to a suffocation hazard. The product violates federal safety standards because it has an incline angle greater than 10 degrees and was marketed for infant sleep, and infant fatalities have been reported in similar inclined sleepers.

    Product
    HONEY JOY Infant Swings
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·23294·2023-09-21

    Shimano 11-Speed Road Cranksets Recalled for Crash Hazard

    Shimano is recalling about 680,000 bonded 11-speed road cranksets because the crank parts can separate and break, posing a crash hazard. Six injuries including bone fractures have been reported.

    Product
    11-Speed Bonded Hollowtech II Road Cranksets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V647000·2023-09-21

    2023 Subaru Driveshaft Center Support Bolts May Loosen

    Subaru is recalling certain 2023 Ascent, Legacy, Impreza, and Outback vehicles because center support bolts for the driveshaft may loosen, potentially causing the driveshaft to disconnect and increasing crash risk. Dealers will clean and replace the bolts at no charge.

    Product
    SUBARU — SUBARU OUTBACK, ASCENT, LEGACY, IMPREZA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23293·2023-09-21

    H&M Men's Clasp Beaded Bracelets Recalled for High Lead Content

    H&M is recalling about 12,290 men's clasp beaded bracelets because the clasp contains lead levels exceeding the federal ban. Lead is toxic if ingested by young children and can cause adverse health effects.

    Product
    Men's clasp beaded bracelets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23291·2023-09-21

    DR Power Chipper Shredders Recalled Due to Laceration Hazard

    DR Power Chipper Shredders are being recalled because metal pieces can come loose and be ejected, or the hopper can detach, both creating laceration hazards. The firm has received 79 reports of parts coming loose and 3 reports of hopper detachment, with a total of 3 reported injuries.

    Product
    DR Power Chipper Shredders
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23793·2023-09-21

    Novaform ComfortGrande and DreamAway Mattresses Recalled for Mold Contamination

    FXI recalls about 48,000 Novaform mattresses from Costco due to mold contamination from water exposure during manufacturing. The mold poses a health risk to people with compromised immune systems or mold allergies. No injuries have been reported.

    Product
    Novaform ComfortGrande 14-inch and Novaform DreamAway 8-inch Mattresses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23292·2023-09-21

    Rainbow Road Series Board Books Recall: Detachable Plastic Rings Choking Hazard

    Make Believe Ideas recalls seven Rainbow Road Series board books because plastic binding rings can detach, posing a choking hazard to young children. About 260,000 units were sold nationwide from March 2022 through August 2023.

    Product
    Rainbow Road Series Board Books
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-2509-2023·2023-09-20

    Abbott Proclaim DRG Implantable Pulse Generators cannot exit MRI mode

    Abbott Medical is recalling approximately 17,394 Proclaim DRG Implantable Pulse Generators worldwide due to reports that patients cannot exit MRI mode on affected devices. This malfunction may prevent normal device operation when mode-switching is needed.

    Product
    Proclaim DRG Implantable Pulse Generator REF 3664 Product Description: The implantable pulse generator (IPG) is an electronic device designed to be connected to one or more extensions or leads with up to 16 electrodes total. It is powered by a hermetically sealed battery…
    Category
    Medical Device
    Distribution
    Distributed nationwide