The Recall Desk

State

Minnesota product recalls

72,907 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.

These figures cover only the 7,804 recalls whose distribution notice names Minnesota specifically. The 72,907 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

1101–1125 of 80711

  • ModerateFDA (Devices)·Z-2526-2026·2026-07-01

    Multi-Snare Set catheter fails biocompatibility requirements

    PFM Medical Inc. is recalling Multi-Snare Set catheters (5 mm and 10 mm sizes) because they failed biocompatibility testing for in-vitro cytotoxicity and could cause localized inflammation and tissue irritation if they contact a patient's blood vessels.

    Product
    Multi-Snare Set: 5 mm x 125 cm, REF: 147305; 10 mm x 125 cm, REF: 147310
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2577-2026·2026-07-01

    Octopus 4 Tissue Stabilizer incorrectly assembled tubing positions

    Medtronic is recalling 590 units of the Octopus 4 Tissue Stabilizer, Model 29400 due to an assembly error where tubing was attached to the wrong positions during manufacturing.

    Product
    Octopus 4 Tissue Stabilizer, Model 29400
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2588-2026·2026-07-01

    Medline 10mL Polycarbonate Colored Syringes Convenience Kits Recalled

    Medline Industries is recalling convenience kits containing 10mL polycarbonate colored syringes due to unapproved design changes made outside of FDA clearance requirements.

    Product
    Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. MAJOR BASIN SET DYNJ85723
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0612-2026·2026-07-01

    Corlanor ivabradine tablets recalled for presence of foreign substance

    Amgen Inc. is recalling Corlanor (ivabradine) 5 mg tablets nationwide due to the presence of a foreign substance. The recall affects approximately 934,577 bottles distributed in the United States.

    Product
    CORLANOR — CORLANOR (IVABRADINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2576-2026·2026-07-01

    Octopus Evolution AS Tissue Stabilizer Model TS2500 Tubing Assembly Issue Recall

    Medtronic is recalling 288 units of the Octopus Evolution AS Tissue Stabilizer Model TS2500 due to incorrect tubing positioning during manufacturing, where short and long tubes were attached to wrong locations.

    Product
    Octopus Evolution AS Tissue Stabilizer, Model TS2500
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2584-2026·2026-07-01

    Medline 10mL Polycarbonate Colored Syringes Convenience Kits Recalled

    Medline Industries is recalling convenience kits containing 10mL polycarbonate colored syringes because the products underwent unapproved design changes outside of FDA clearance.

    Product
    Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. DR G'S BREAST PACK DYNJ51124B LIPO SUPPLEMENT PACK-LF DYNJ0341174D PLASTIC PACK DYNJ66746 DYNJ85702
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2595-2026·2026-07-01

    Medline 10mL Polycarbonate Colored Syringes in Convenience Kits Recalled

    Medline Industries is recalling convenience kits containing 10mL polycarbonate colored syringes because the products contain unapproved design changes that were not cleared by the FDA.

    Product
    Convenience kits containing select SKUs of 10mL Polycarbonate Colored Syringes. PICC LINEPACK (PCLUI)642-LF DYNJ47717A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2554-2026·2026-07-01

    Thuvera Laser Console Software Version 2.2 Recall Notice

    IPG Medical Corporation is recalling the Thuvera Laser Console (Software Version 2.2) due to a software anomaly that causes false display of error code 5018. The defect affects 198 units distributed nationwide in Massachusetts.

    Product
    Thuvera Laser Console. Software Version 2.2. Portable Thulium Fiber Laser.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0619-2026·2026-07-01

    Hydroxyzine Hydrochloride Oral Solution recalled for foreign substance

    ANI Pharmaceuticals is recalling Hydroxyzine Hydrochloride Oral Solution due to the presence of a foreign substance. The affected lot is S25133A, distributed nationwide.

    Product
    HYDROXYZINE HYDROCHLORIDE — HYDROXYZINE HYDROCHLORIDE (HYDROXYZINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V417000·2026-06-30

    Ford Recalls 2021-2023 Mustang Mach E for Rear Differential Defect

    Ford is recalling 2021-2023 Mustang Mach E vehicles because the rear differential pinion shaft may fracture, potentially causing loss of drive power or unintended movement.

    Product
    FORD — FORD MUSTANG MACH E
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V414000·2026-06-30

    Chrysler Recalls 2026 Jeep Grand Wagoneer Models for Brake Software Defect

    Chrysler is recalling 2026 Jeep Grand Wagoneer and Grand Wagoneer L vehicles because brake software may disable stability control and brake assist, increasing crash risk.

    Product
    JEEP — JEEP GRAND WAGONEER, GRAND WAGONEER L
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V413000·2026-06-30

    Chrysler Recalls Jeep Models Due to Missing Gear Indicator Software Error

    Chrysler is recalling specific 2022-2024 Jeep models because a software error may cause the transmission gear selection indicator to fail to display.

    Product
    JEEP — JEEP WAGONEER L, GRAND CHEROKEE, WAGONEER, GRAND CHEROKEE L
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V418000·2026-06-30

    2025 Ford Mustang windshield wiper and washer system failure recall

    Ford is recalling certain 2024–2026 Mustang and 2025–2026 Mustang GTD vehicles because the windshield wipers may function only at high speed and the washing system may fail during cold temperatures, reducing visibility and increasing crash risk.

    Product
    FORD — FORD MUSTANG, MUSTANG GTD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V420000·2026-06-30

    Teko Recalls 2026 Electric Vehicles for Missing Pedestrian Warning System

    Teko is recalling 2026 Triumph, Trophy, Trophy Plus, Turbo, and TurboLite vehicles because the acoustic vehicle alerting system may be missing, increasing pedestrian crash risk.

    Product
    TEKO — TEKO TROPHY PLUS, TURBOLITE, TURBO, TROPHY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V416000·2026-06-30

    Jayco Recalls 2027 Motorhomes Due to Missing Dinette Brackets

    Jayco is recalling 2027 Entegra Accolade and Seneca motorhomes because missing front brackets allow the dinette to shift, increasing injury risk.

    Product
    ENTEGRA — ENTEGRA, JAYCO ACCOLADE, SENECA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26E039000·2026-06-30

    Nissan Recalls JATCO Transaxles for Gear Indicator Display Failure

    Nissan is recalling specific JATCO automatic transmission assemblies because a hardware failure may cause the gear shifter indicator to display incorrectly, increasing crash risk.

    Product
    POWER TRAIN:AUTOMATIC TRANSMISSION recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V419000·2026-06-30

    2026 Nissan Rogue Transmission Gear Indicator Display Failure

    Nissan is recalling certain 2026 Rogue vehicles because the instrument panel may not display the transmission gear selection indicator, potentially leading to unintended vehicle movement or rollaway.

    Product
    NISSAN — NISSAN ROGUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V412000·2026-06-29

    Tiffin Motorhomes Recreational Vehicles Rooftop Fan Fire Risk Recall

    Tiffin Motorhomes is recalling certain 2026–2027 recreational vehicles with MaxxAir N-Series Maxxfan rooftop ventilation fans. The circuit board may overheat and increase the risk of fire.

    Product
    TIFFIN — TIFFIN ALLEGRO BREEZE, WAYFARER, ALLEGRO RED, BYWAY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·26V411000·2026-06-29

    Jayco Recalls 2024 Alante and Vision RVs for Incorrect Weight Labels

    Jayco is recalling 2024 Alante and Entegra Vision recreational vehicles because the occupant and cargo capacity labels may list incorrect weights, potentially leading to vehicle overloading.

    Product
    JAYCO — JAYCO, ENTEGRA ALANTE, VISION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V410000·2026-06-26

    Nissan Recalls 2025 Sentra Vehicles for Driveshaft Defect

    Nissan is recalling 2025 Sentra vehicles because a front left driveshaft may not be fully seated, risking transmission fluid leaks and loss of drive power.

    Product
    NISSAN — NISSAN SENTRA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V407000·2026-06-26

    Thomas Built School Bus Recall for Door Switch Failure

    Daimler Trucks is recalling 2026-2027 Thomas Built school buses because the entrance door may fail to open or close, increasing injury risk in a crash.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER HDX2, SAF-T-LINER EFX2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V408000·2026-06-26

    Thomas Built Buses Recalls SAF-T-LINER HDX2 Due to Door Malfunction

    Daimler Trucks North America is recalling 2026-2027 Thomas Built SAF-T-LINER HDX2 buses because the entrance door may fail to open or close, increasing injury risk in crashes.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER HDX2
    Category
    Vehicle
    Distribution
    Distributed nationwide