The Recall Desk

State

Minnesota product recalls

72,936 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 72,936 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

2901–2925 of 80740

  • ModerateFDA (Devices)·Z-1549-2026·2026-03-18

    Medartis APTUS 2.5 TriLock screw lots mixed with 2.8 mm

    Medartis is recalling one lot of the APTUS 2.5 TriLock Screw 16 mm because of a mix up between specified lots of 2.5 mm and 2.8 mm outer diameter screws.

    Product
    Brand Name: APTUS Product Name: 2.5 TriLock Screw 16mm, HD7, 1/Pkg Model/Catalog Number: A-5750.16/1 Software Version: Not applicable. Product Description: The APTUS fixation systems are used for fractures, osteotomies and arthrodesis of the hand, forearm, shoulder and foot.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1561-2026·2026-03-18

    Bisaf Strep A self-test recalled because it lacks FDA clearance

    Altruan GmbH is recalling the Bisaf Strep A Self-Test, used to detect group A streptococcal antigens in throat swabs, because the product is not cleared by the FDA.

    Product
    Brand Name: Bisaf Strep A Self-Test. Test for detection of group A streptococcal antigens in throat swabs.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1550-2026·2026-03-18

    Medartis APTUS TriLock screw lots mixed 2.5 mm and 2.8 mm

    Medartis is recalling one lot of the APTUS 2.8 TriLock Screw 16 mm because of a mix up between specified lots of 2.5 mm and 2.8 mm outer diameter screws.

    Product
    Brand Name: APTUS Product Name: 2.8 TriLock Screw 16mm, HD7, 1/Pkg Model/Catalog Number: A-5850.16/1 Software Version: Not applicable. Product Description: The APTUS fixation systems are used for fractures, osteotomies and arthrodesis of the hand, forearm, shoulder and foot.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1560-2026·2026-03-18

    Clearest Strep-A cassette test recalled because it lacks FDA clearance

    Altruan GmbH is recalling the Clearest Strep-A Cassette Test, used to detect group A streptococci in throat swab samples, because the product is not cleared by the FDA.

    Product
    Clearest Strep-A Cassette Test. Test to determine the presence of group A streptococci (Strep A) in throat swab samples.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1496-2026·2026-03-18

    BD syringe batch may contain Luer Slip instead of Luer Lok

    Becton Dickinson is recalling one lot of 10 mL Non-Sterile BD Luer-Lok Tip Syringes because some Luer Slip syringes were incorrectly included in a batch designated for Luer Lok syringes.

    Product
    10mL Non-Sterile BD Luer-Lok Tip Syringe Only. Catalog Number: 301029. 850 bulk non-sterile units per case.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1559-2026·2026-03-18

    Wondfo Streptococcal A self-test recalled because it lacks FDA clearance

    Altruan GmbH is recalling the Wondfo Streptococcal A At-Home Self-Test, used for group A beta-hemolytic streptococcal infection, because the product is not cleared by the FDA.

    Product
    Wondfo Streptococcal A At-Home Self-Test. At-home test for group A beta-hemolytic streptococcal infection.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Food)·H-0545-2026·2026-03-18

    C2O Coconut Water with Pulp 15-pack with incorrect outer box labels

    The outer cardboard box of C2O Coconut Water with Pulp (17.5 oz) 15-packs contains incorrect Nutrition Facts and Ingredient Lists that fail to disclose 5g of added sugar per can, although the can itself has correct labeling.

    Product
    C2O Coconut Water with Pulp (17.5 oz) 15 Pack UPC: 8-50274-00792-8
    Category
    Food
    Distribution
    11 states
  • LowFDA (Devices)·Z-1505-2026·2026-03-18

    Penner bathing spa models recalled for lacking a unique device identifier

    Penner Patient Care is recalling Pacific Bathing Spa models 390010-1, 390010-X and 390010-2 because the device does not bear a unique device identifier.

    Product
    Penner Pacific Bathing Spa, Model Numbers 390010-1, 390010-X, 390010-2
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1499-2026·2026-03-18

    Penner bathing spa 350010 series recalled for lacking unique device identifier

    Penner Patient Care is recalling Pacific Bathing Spa models in the 350010 series because the device does not bear a unique device identifier.

    Product
    Penner Pacific Bathing Spa, Model Numbers 350010-1, 350000-2, 350010-X
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1500-2026·2026-03-18

    Penner bathing spa 360010 series recalled for lacking device identifier

    Penner Patient Care is recalling Pacific Bathing Spa models across the 360010, 362010 and 370000 series because the device does not bear a unique device identifier.

    Product
    Penner Pacific Bathing Spa, Model Numbers 360010-2WT, 360010-1, 370000-1W, 360010-1WT, 362010-1, 370000-1WL, 360010-1L, 360010-1W, 360010-XWTL, 370000-XWL, 360010-1WTL, 360010-XWT, 360010-2, 370000-2W, 360010-2L, 370000-2WL, 360010-X, 370000-XW, 360010-2W, 362010-2, 360010, 37000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1504-2026·2026-03-18

    Penner bathing spa 361910 series recalled for lacking unique device identifier

    Penner Patient Care is recalling Pacific Bathing Spa models in the 361910 series because the device does not bear a unique device identifier.

    Product
    Penner Pacific Bathing Spa, Model Numbers 361910-1A, 361910-1A, 361910-XA, 361910-2I, 361910-1A, 361910-1, 361910-XI, 361910-1I, 361910-2A, 36191-1A, 361910-X
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1503-2026·2026-03-18

    Penner bathing spa 360030 series recalled for lacking unique device identifier

    Penner Patient Care is recalling Pacific Bathing Spa models in the 360030 series because the device does not bear a unique device identifier.

    Product
    Penner Pacific Bathing Spa, Model Numbers 360030-1C, 360030-1CE, 360030-1CTS, 360030-XCE, 360030-XC, 360030-1CT, 360030-1C, 360030-XC, 360030-XCT, 360030-1CTS, 360030-XCTS, 3600301-CTS, 360030-XCE, 360030-1CT, 360030-1CE, 36030-XCT
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1506-2026·2026-03-18

    Penner bathing spa 560010 series recalled for lacking unique device identifier

    Penner Patient Care is recalling Pacific Bathing Spa models in the 560010 series because the device does not bear a unique device identifier.

    Product
    Penner Pacific Bathing Spa, Model Numbers 560010-2L, 560010-XL, 560010-1L, 560010-XL
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1501-2026·2026-03-18

    Penner Pacific bathing spa 360020-1EP lacks a unique device identifier

    Penner Patient Care is recalling Pacific Bathing Spa model 360020-1EP because the device does not bear a unique device identifier.

    Product
    Penner Pacific Bathing Spa, Model Numbers 360020-1EP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1507-2026·2026-03-18

    Penner bathing spa 760010 and 770010 lack unique device identifiers

    Penner Patient Care is recalling Pacific Bathing Spa models 760010-1 and 770010-1 because the device does not bear a unique device identifier.

    Product
    Penner Pacific Bathing Spa, Model Numbers 760010-1, 770010-1
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V158000·2026-03-17

    Ford Super Duty high pressure fuel pump may fail from biodiesel deposits

    Ford is recalling certain 2020-2022 F-Super Duty and related vehicles previously repaired under recall 24V957 because biodiesel deposits may form on pump drivetrain rollers, leading to fuel pump failure.

    Product
    FORD — FORD F-750, F-250 SD, F-550 SD, F-600 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V159000·2026-03-17

    Ford Explorer second-row seat belt anchor bolts may be improperly secured

    Ford is recalling certain 2020-2026 Explorer and Lincoln Aviator vehicles because the seat belt anchor bolts at the second-row outer seating positions may be improperly secured.

    Product
    LINCOLN — LINCOLN, FORD AVIATOR, EXPLORER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·26V160000·2026-03-17

    2026 Hyundai Palisade power rear seats may fail to detect occupants

    Hyundai is recalling 2026 Palisade and Palisade Hybrid vehicles with Limited or Calligraphy trim because the second and third row power seats may fail to detect a person and continue moving, risking entrapment or injury.

    Product
    HYUNDAI — HYUNDAI PALISADE HYBRID, PALISADE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V155000·2026-03-17

    Ford F-59 brake lights may stay illuminated when brakes released

    Ford is recalling certain 2025-2026 F-59 and F-53 commercial stripped chassis vehicles because the exterior brake lights may remain illuminated when the driver is not applying the brakes.

    Product
    FORD — FORD F-59, F-53
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V157000·2026-03-17

    2026 Ford Maverick vehicles recalled for moonroof glass detachment risk

    Ford is recalling certain 2025–2026 Maverick vehicles because the moonroof glass may not be bonded correctly to the frame and could detach, becoming a road hazard and increasing crash risk.

    Product
    FORD — FORD MAVERICK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V153000·2026-03-16

    Orange EV Recalls Terminal Trucks Due to Foldaway Seat Failure Risk

    Orange EV is recalling 2022-2026 terminal trucks because the optional foldaway training seat may fail, potentially failing to restrain occupants during a crash.

    Product
    ORANGE EV — ORANGE EV E-TRIEVER, T-SERIES ELECTRIC TRUCK, HUSK-E
    Category
    Vehicle
    Distribution
    Distributed nationwide