The Recall Desk

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.

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.

3501–3525 of 83201

  • ModerateFDA (Devices)·Z-1229-2026·2026-02-11

    Prismaflex HF1000 set 107140 recalled over a dislodging deaeration chamber

    Vantive US Healthcare is recalling 93,576 Prismaflex HF1000 Sets, product code 107140, because the deaeration chamber may dislodge from the Prismaflex Control Unit.

    Product
    PRISMAFLEX HF1000 SET, Product Code 107140; Dialyzer, High Permeability With Or Without Sealed Dialysate System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1268-2026·2026-02-11

    CleverCut sphincterotomes recalled over a skipped thermoforming step

    Olympus is recalling the CleverCut Single Use 3-Lumen Sphincterotome V, model KD-V411M-0320, because devices which did not undergo thermoforming could deform and lose performance.

    Product
    Brand Name: CleverCut Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-0320; Software Version: N/A Product Description: These instruments have been designed to be used with an Olympus endoscope and guidewire for papillotomy using high-frequency
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1240-2026·2026-02-11

    NAEOTOM Alpha software applications recalled because they lack FDA clearance

    Siemens is removing three software applications from 88 NAEOTOM Alpha CT systems because the applications have not received FDA 510(k) clearance.

    Product
    NAEOTOM Alpha Software applications: syngo.CT Brain Quantification syngo.CT Vessel Hyperdensities syngo.CT ASPECTS
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1289-2026·2026-02-11

    Sphincterotome KD-401Q-0730 recalled over a skipped thermoforming step

    Olympus is recalling the Disposable Triple Lumen Sphincterotome, model KD-401Q-0730, because devices which did not undergo thermoforming could deform and lose performance.

    Product
    Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number: KD-401Q-0730 Product Description: These instruments have been designed to be used with an Olympus endoscope and guidewire for papillotomy using high-frequency current.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1295-2026·2026-02-11

    Sphincterotome KD-V411M-3020 recalled over a skipped thermoforming step

    Olympus is recalling the Single Use 3-Lumen Sphincterotome V, model KD-V411M-3020, because devices which did not undergo thermoforming could deform and lose performance.

    Product
    Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-3020 Product Description: These instruments have been designed to be used with an Olympus endoscope and guidewire for papillotomy using high-frequency current.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1279-2026·2026-02-11

    Sphincterotome KD-VC411Q-0730 recalled over a skipped thermoforming step

    Olympus is recalling the Single Use 3-Lumen Sphincterotome V (Distal Wire guided), model KD-VC411Q-0730, because devices which did not undergo thermoforming could deform and lose performance.

    Product
    Product Name: Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model/Catalog Number: KD-VC411Q-0730; Software Version: N/A Product Description: These instruments have been designed to be used with an Olympus endoscope and guidewire for papillotomy using high-frequency
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1291-2026·2026-02-11

    Sphincterotome KD-V411M-1530 recalled over a skipped thermoforming step

    Olympus is recalling the Single Use 3-Lumen Sphincterotome V, model KD-V411M-1530, because devices which did not undergo thermoforming could deform and lose performance.

    Product
    Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-1530 Product Description: These instruments have been designed to be used with an Olympus endoscope and guidewire for papillotomy using high-frequency current.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1272-2026·2026-02-11

    Sphincterotome KD-V411M-0720 recalled over a skipped thermoforming step

    Olympus is recalling the Single Use 3-Lumen Sphincterotome V, model KD-V411M-0720, because devices which did not undergo thermoforming could deform and lose performance.

    Product
    Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-0720; Software Version: N/A Product Description: These instruments have been designed to be used with an Olympus endoscope and guidewire for papillotomy using high-frequency current.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1241-2026·2026-02-11

    CT software applications recalled because they lack FDA clearance

    Siemens is removing three software applications from five NAEOTOM Alpha.Prime CT systems because the applications have not received FDA 510(k) clearance.

    Product
    NAEOTOM Alpha.Prime Software applications: syngo.CT Brain Quantification syngo.CT Vessel Hyperdensities syngo.CT ASPECTS
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·26T006000·2026-02-10

    Vee Tyre Recalls Taiga AT Tires Due to Sidewall Separation Risk

    Vee Tyre is recalling specific Taiga AT tires because the sidewall and inner liner may crack and separate, increasing the risk of a crash.

    Product
    TIRES:SIDEWALL recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V076000·2026-02-10

    2024–2027 Volvo VNL (4) trucks recalled for inadequate parking brake

    Volvo Trucks is recalling certain 2024–2027 VNL (4) vehicles lacking auxiliary parking brakes, which can result in inadequate parking brake force and rollaway risk.

    Product
    VOLVO — VOLVO VNL (4)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V075000·2026-02-09

    Harley-Davidson Sportster S upper triple clamp may fracture during use

    Harley-Davidson is recalling certain 2021-2026 RH1250S Sportster S motorcycles because the upper triple clamp may fracture, which can lead to a loss of control.

    Product
    HARLEY-DAVIDSON — HARLEY-DAVIDSON RH1250S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V074000·2026-02-08

    Oshkosh Recalls 2025-2026 NGDV Vehicles Due to Brake Pedal Defect

    Oshkosh is recalling 2025-2026 NGDV and NGDV Electric vehicles because the brake pedal mounting pin and clip may be missing, risking loss of braking ability.

    Product
    OSHKOSH — OSHKOSH NGDV ELECTRIC, NGDV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V070000·2026-02-06

    Mercedes-Benz Metris air bag control unit may accumulate water

    Daimler Vans USA is recalling certain 2020 and 2022-2023 Mercedes-Benz Metris right-hand-drive vehicles because water may accumulate on the air bag control unit and stop the air bags deploying as intended.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ METRIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V073000·2026-02-06

    Mercedes-Benz EQB high voltage battery may fail internally and catch fire

    Mercedes-Benz is recalling certain 2022-2024 EQB vehicles because the high voltage battery may fail internally and lead to a vehicle fire while parked or driving. Owners are advised to park outside.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ EQB 350 4MATIC, EQB 300 4MATIC, EQB 250+
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V072000·2026-02-06

    Volvo Recalls 2017 S60L Vehicles Due to Door Latch Defect

    Volvo is recalling 2,758 2017 S60L vehicles because a door latch component may break, preventing the door from latching securely and increasing injury risk.

    Product
    VOLVO — VOLVO S60L
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V067000·2026-02-05

    Jaguar I-PACE high voltage battery may overheat increasing fire risk

    Jaguar is recalling certain 2020-2021 I-PACE vehicles because the high voltage battery may overheat. Owners are advised to park and charge outside and limit charging to 90%.

    Product
    JAGUAR — JAGUAR I-PACE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·26253·2026-02-05

    Outdoor chairs and barstools recalled after reports of legs bending

    About 158,486 Lancaster Table & Seating powder-coated aluminum outdoor chairs and barstools are being recalled because the legs can bend or break while in use.

    Product
    Lancaster Table & Seating Powder-Coated Aluminum Outdoor Chairs and Barstools
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·26250·2026-02-05

    PurSteam steamers recalled after reports of burns from expelled hot water

    About 75,400 PurSteam Elite Travel Steamers and about 119,000 PurSteam Mighty Lil Steamers are being recalled because they can expel hot water from the steam nozzle during use.

    Product
    PurSteam Mighty Lil Steamers and PurSteam Elite Travel Steamers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26246·2026-02-05

    Kitosun submersible LED lights recalled over accessible coin batteries

    About 8,100 Kitosun Submersible LED Lights are being recalled because they contain lithium coin batteries that children can access easily and lack the warnings required by Reese's Law.

    Product
    Kitosun Submersible LED Lights
    Category
    Consumer Product
    Distribution
    Distributed nationwide