The Recall Desk

State

Minnesota product recalls

72,940 recalls have nationwide distribution and so reach Minnesota. 7,804 additional recalls listed Minnesota specifically in their distribution scope.

What the numbers show

Total
7,804
Critical
1,125
Severe
1,892
Most recent
2026-09-09

Of the 7,804 recalls naming Minnesota we have scored against our rubric, 1,125 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,892 (24%) are Severe.

Which agencies issued them

These figures cover only the 7,804 recalls whose distribution notice names Minnesota specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

3451–3475 of 80744

  • ModerateFDA (Devices)·Z-1274-2026·2026-02-11

    Sphincterotome KD-V411M-0730 recalled over a skipped thermoforming step

    Olympus is recalling the Single Use 3-Lumen Sphincterotome V, model KD-V411M-0730, 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-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 current.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1225-2026·2026-02-11

    Prismaflex ST150 sets recalled over a deaeration chamber that may dislodge

    Vantive US Healthcare is recalling 264,040 units of the PRISMAFLEX ST150 SET US because the Prismaflex Set deaeration chamber may dislodge from the Prismaflex Control Unit.

    Product
    PRISMAFLEX ST150 SET US, Product Code 107640US; Dialyzer, High Permeability With Or Without Sealed Dialysate System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1254-2026·2026-02-11

    Illuminated depressors recalled with no reason given in the record

    Vortex Surgical is recalling the TID Pharos Illuminated Depressor, VS0801B. The reason field in the enforcement record reads only "XXX", so no hazard is stated.

    Product
    Vortex Surgical TID Pharos Illuminated Depressor, VS0801B
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1273-2026·2026-02-11

    Single use 3-lumen sphincterotomes recalled over a skipped thermoforming step

    Olympus is recalling the Single Use 3-Lumen Sphincterotome V, model KD-V411M-0725, 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-0725; 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-1280-2026·2026-02-11

    Sphincterotome KD-VC411Q-0320 recalled over a skipped thermoforming step

    Olympus is recalling the Single Use 3-Lumen Sphincterotome V (Distal Wire guided), model KD-VC411Q-0320, 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-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-1231-2026·2026-02-11

    Prismaflex TPE2000 sets recalled over a deaeration chamber that may dislodge

    Vantive US Healthcare is recalling 13,760 units of the PRISMAFLEX TPE2000 SET because the Prismaflex Set deaeration chamber may dislodge from the Prismaflex Control Unit.

    Product
    PRISMAFLEX TPE2000 SET, Product Code 114093; Dialyzer, High Permeability With Or Without Sealed Dialysate System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1276-2026·2026-02-11

    Sphincterotome KD-V431M-0730 recalled over a skipped thermoforming step

    Olympus is recalling the Single Use 3-Lumen Sphincterotome V, model KD-V431M-0730, 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-V431M-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 current.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1275-2026·2026-02-11

    Sphincterotome KD-V431M-0720 recalled over a skipped thermoforming step

    Olympus is recalling the Single Use 3-Lumen Sphincterotome V, model KD-V431M-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-V431M-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
  • ModerateFDA (Devices)·Z-1310-2026·2026-02-11

    Hoist sling bars recalled after a lifting bar mounting bolt broke

    ETAC A/S is recalling 64 units of Molift 2-point sling bars, accessories to mobile hoists after a customer reported the bolt for mounting the lifting bar breaking during assembly and load testing.

    Product
    Brand Name: Molift Product Name: Molift 2-point sling bars (Accessory to mobile hoists) Model/Catalog Numbers: (1) 1530101, (2) 1530102 Product Description: The mobile hoist is an assistive device intended for alleviation of, or compensation for, a functional, impairment due t
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1300-2026·2026-02-11

    Bubble sensors recalled over connecting cables that can be damaged

    Maquet Cardiopulmonary is recalling 3,050 Bubble Sensors because excessive bending of the connecting cable can damage the Venous Bubble Sensor or cause loose cable contact.

    Product
    Bubble Sensor for 3/8" x 3/32" tubing; Model Number: 701055720;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1284-2026·2026-02-11

    Sphincterotome KD-VC433Q-0730 recalled over a skipped thermoforming step

    Olympus is recalling the Single Use 3-Lumen Sphincterotome V (Distal Wire guided), model KD-VC433Q-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-VC433Q-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 c
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1287-2026·2026-02-11

    Sphincterotome KD-401Q-0330 recalled over a skipped thermoforming step

    Olympus is recalling the Disposable Triple Lumen Sphincterotome, model KD-401Q-0330, because devices which did not undergo thermoforming could deform and lose performance.

    Product
    Product Name: Disposable Triple Lumen Sphincterotome Model/Catalog Number: KD-401Q-0330 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-1297-2026·2026-02-11

    Sphincterotome KD-VC411Q-0725 recalled over a skipped thermoforming step

    Olympus is recalling the Single Use 3-Lumen Sphincterotome V (Distal Wire guided), model KD-VC411Q-0725, 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-0725; 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-1282-2026·2026-02-11

    Sphincterotome KD-VC412Q-0215 recalled over a skipped thermoforming step

    Olympus is recalling the Single Use 3-Lumen Sphincterotome V (Distal Wire guided), model KD-VC412Q-0215, 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-VC412Q-0215; 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-1278-2026·2026-02-11

    Distal wire guided sphincterotomes recalled over a skipped thermoforming step

    Olympus is recalling the Single Use 3-Lumen Sphincterotome V (Distal Wire guided), model KD-VC411Q-0720, 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-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
    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·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·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 250+, EQB 350 4MATIC, EQB 300 4MATIC
    Category
    Vehicle
    Distribution
    Distributed nationwide