The Recall Desk

State

Minnesota product recalls

73,737 recalls have nationwide distribution and so reach Minnesota. 7,849 additional recalls listed Minnesota specifically in their distribution scope.

What the numbers show

Total
7,849
Critical
1,137
Severe
2,245
Most recent
2026-10-28

Of the 7,849 recalls naming Minnesota we have scored against our rubric, 1,137 (14%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,245 (29%) are Severe.

These figures cover only the 7,849 recalls whose distribution notice names Minnesota specifically. The 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

32826–32850 of 81586

  • ModerateFDA (Devices)·Z-1375-2020·2020-03-04

    Biomet 3i Recalls Bellatek Encode Healing Abutments Due to Rotation Error

    Biomet 3i is recalling specific Bellatek Encode Healing Abutments because they may cause incorrect rotation and margin misalignment in dental impressions.

    Product
    CERTAIN BELLATEK ENCODE HEALING ABUTMENT 4.1MM(D) X 5MM(P) X 3MM(H) Reference Number: IEHA453
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1380-2020·2020-03-04

    Biomet 3i Recalls Bellatek Encode Healing Abutments Due to Data Errors

    Biomet 3i is recalling specific Bellatek Encode Healing Abutments because they produce incorrect rotation and margin contour data during scanning.

    Product
    CERTAIN BELLATEK ENCODE HEALING ABUTMENT 4.1MM(D) X 6MM(P) X 6MM(H) Reference Number: IEHA466
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0784-2020·2020-03-04

    Lifetime Fitness D. Tox Shake Mix Recalled for Unapproved Herbicide

    Pro-Form Manufacturing LLC is recalling Lifetime Fitness D. Tox Shake Mix because the flax seed used in the product contains an unapproved herbicide.

    Product
    Lifetime Fitness D. Tox Shake Mix; Plant-Based Protein Blend. Dietary Supplement - Net Wt. 2.50 lb. (40 oz.) 1.13 kg One gallon White HDPE Jar Natural Chocolate Flavor UPC: 6 82471 00830-5 Product number: 6142-2644 Manufactured exclusively for: Life Time Fitness Inc.…
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Food)·F-0747-2020·2020-03-04

    Domino Foods Recalls Great Value Light Brown Sugar for Foreign Material

    Domino Foods Inc is recalling Great Value Light Brown Sugar, 32 oz, due to possible foreign material. The product was distributed to 23 states and Saudi Arabia.

    Product
    Great Value Light Brown Sugar, 32 oz (2 LB) plastic bag, UPC 078742372211, Lots 50043 (Best By Jan 22, 2022), 50044 (Best By Jan 23, 2022), 50045 (Best By Jan 24, 2022), 50046 (Best By Jan 25, 2022), 50047 (Best By Jan 26, 2022)
    Category
    Food
    Distribution
    23 states
  • ModerateFDA (Food)·F-0778-2020·2020-03-04

    Nature's Sunshine SmartMeal Shake Mix Recalled for Unapproved Herbicide in Flax Seed

    Pro-Form Manufacturing LLC is recalling Nature's Sunshine SmartMeal Nutritional Shake Mix because the flax seed used in the product contains an unapproved herbicide.

    Product
    Nature's Sunshine SmartMeal Nutritional Shake Mix; Natural Chocolate Flavor Net Wt. 1 lb. 3.5 oz. (555 Grams) UPC: 0 99904 03084 8 Product number: 6116 US3084 Distributed exclusively by: Nature's Sunshine Products, Inc. Spanish Fork, UT 84660
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-1367-2020·2020-03-04

    Biomet 3i Recalls Bellatek Encode Healing Abutments Due to Data Misalignment

    Biomet 3i is recalling specific Bellatek Encode Healing Abutments because they produce incorrect rotation and margin contour data.

    Product
    CERTAIN¿ BELLATEK ENCODE HEALING ABUTMENT 3.4MM(D) X 3.8MM(P) X 4MM(H) Reference Number: IEHA344
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1368-2020·2020-03-04

    Biomet 3i Recalls Bellatek Encode Healing Abutments Due to Data Errors

    Biomet 3i is recalling specific Bellatek Encode Healing Abutments because they produce incorrect rotation and margin contour data during scanning.

    Product
    CERTAIN BELLATEK ENCODE HEALING ABUTMENT 3.4MM(D) X 3.8MM(P) X 6MM(H) Reference Number: IEHA346
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0744-2020·2020-03-04

    Domino Brown Sugar Recalled for Possible Foreign Material

    Domino Foods Inc is recalling specific lots of Domino Premium Pure Cane Light Brown Sugar due to possible foreign material.

    Product
    Domino Premium Pure Cane Light Brown Sugar, 16 oz (1 LB) box, UPC 049200056752, Lots 50045 (Best By Jan 24, 2022) & 50046 (Best By Jan 25, 2022)
    Category
    Food
    Distribution
    23 states
  • ModerateFDA (Devices)·Z-1364-2020·2020-03-04

    Exactech Recalls Truliant Splined Stem Extensions Due to Labeling Error

    Exactech is recalling four Truliant Splined Stem Extensions because the labels incorrectly identify the implant size as 17mm x 80mm instead of 18mm x 120mm.

    Product
    Truliant Splined Stem Extension, 18mm x 120mm - Product Usage: The devices are used in a cemented total knee prosthesis system, which provides femoral components, tibial inserts, stems, augments, and surgical instrumentation for use in primary and revision total knee…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1386-2020·2020-03-04

    Biomet 3i Recalls Bellatek Encode Healing Abutments Due to Rotation Error

    Biomet 3i, LLC is recalling specific Bellatek Encode Healing Abutments because they produce incorrect rotation and margin contour misalignment in scanned data.

    Product
    CERTAIN BELLATEK ENCODE HEALING ABUTMENT 5MM(D) X 6MM(P) X 4MM(H) Reference Number: IEHA564
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1385-2020·2020-03-04

    Biomet 3i Recalls Bellatek Encode Healing Abutments Due to Rotation Error

    Biomet 3i, LLC is recalling specific Bellatek Encode Healing Abutments because they may produce incorrect rotation and margin contour misalignment in scanned data.

    Product
    CERTAIN BELLATEK ENCODE HEALING ABUTMENT 5MM(D) X 6MM(P) X 4MM(H) Reference Number: IEHA564
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1388-2020·2020-03-04

    Biomet 3i Recalls Bellatek Encode Healing Abutments Due to Rotation Error

    Biomet 3i is recalling specific Bellatek Encode Healing Abutments because they produce incorrect rotation and margin contour misalignment in dental impressions.

    Product
    CERTAIN BELLATEK ENCODE HEALING ABUTMENT 5MM(D) X 7.5MM(P) X 4MM(H) Reference Number: IEHA574
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0783-2020·2020-03-04

    Lifetime Fitness D. Tox Shake Mix Recalled for Unapproved Herbicide

    Pro-Form Manufacturing LLC is recalling Lifetime Fitness D. Tox Shake Mix because the flax seed used in the product contains an unapproved herbicide.

    Product
    Lifetime Fitness D. Tox Shake Mix; Plant-Based Protein Blend. Dietary Supplement - Net Wt. 2.36 lb. (37.76 oz.) 1.07 kg Program Kit - Natural Vanilla Flavor UPC: 6 82471 00831-2 Product number: 6142-2646 Manufactured exclusively for: Life Time Fitness Inc. 2902…
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-1371-2020·2020-03-04

    Biomet 3i Recalls Bellatek Encode Healing Abutments Due to Misalignment

    Biomet 3i is recalling specific Bellatek Encode Healing Abutments because they may cause incorrect rotation and margin contour misalignment in dental impressions.

    Product
    CERTAIN BELLATEK ENCODE HEALING ABUTMENT 3.4MM(D) X 5MM(P) X 6MM(H) Reference Number: IEHA356
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1387-2020·2020-03-04

    Biomet 3i Recalls Bellatek Encode Healing Abutments Due to Rotation Error

    Biomet 3i is recalling specific Bellatek Encode Healing Abutments because they may cause incorrect rotation and margin misalignment in dental impressions.

    Product
    CERTAIN BELLATEK ENCODE HEALING ABUTMENT 5MM(D) X 6MM(P) X 6MM(H) Reference Number: IEHA566
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1379-2020·2020-03-04

    Biomet 3i Recalls Bellatek Encode Healing Abutments Due to Data Errors

    Biomet 3i is recalling specific Bellatek Encode Healing Abutments because the resulting impression or scanned data may cause incorrect rotation and margin contour misalignment.

    Product
    CERTAIN BELLATEK ENCODE HEALING ABUTMENT 4.1MM(D) X 6MM(P) X 4MM(H) Reference Number: IEHA464
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0779-2020·2020-03-04

    Nature's Sunshine NutriSmart Vanilla Powder Recalled for Unapproved Herbicide

    Pro-Form Manufacturing LLC is recalling Nature's Sunshine NutriSmart Vanilla Powder because the flax seed ingredient contains an unapproved herbicide.

    Product
    Nature's Sunshine NutriSmart Polvo Para Preparar Bebida Sabor Vainilla Con In Toque Sabor a Chocolate; Vainilla Flavor Contenido Neto 510 g UPC: 0 99904 61532 8 Product number: 6116-MX61532 Importado y Distribuido por: Nature's Sunshine Products de Mexico, S.A. de C.…
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-1349-2020·2020-03-04

    Randox RX Daytona Plus Clinical Chemistry Analyzer Software Recall

    Randox Laboratories is recalling RX Daytona Plus clinical chemistry analyzers to fix software issues causing incorrect sample ordering and quality control flags.

    Product
    RX Daytona Plus (with ISE/without ISE); Models Nos. RX4040 (w/ISE) and RX4041 (without ISE) - Product Usage: A fully automated, random access, clinical chemistry analyzer complete with dedicated analyzer software. For use in clinical laboratories.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1363-2020·2020-03-04

    Siemens ADVIA Chemistry Lipase Recalled for Calibration Failures

    Siemens Healthcare Diagnostics is recalling ADVIA Chemistry Lipase reagents due to customer complaints about failed calibrations and increased imprecision in quality control and patient samples.

    Product
    ADVIA Chemistry Lipase, Ref. No. 01984894 B01-4840-01, Siemens Material No. 10311896, UDI 00630414482446 - Product Usage: Lipase measurements are used in the diagnosis and treatment of diseases of the pancreas, such as acute pancreatitis and obstruction of the pancreatic duct.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1382-2020·2020-03-04

    Biomet 3i Recalls Bellatek Encode Healing Abutments Due to Data Errors

    Biomet 3i is recalling specific Bellatek Encode Healing Abutments because they produce incorrect rotation and margin contour data.

    Product
    CERTAIN BELLATEK ENCODE HEALING ABUTMENT 5MM(D) X 5.6MM(P) X 3MM(H) Reference Number: IEHA553
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0745-2020·2020-03-04

    Domino Brown Sugar Recalled for Possible Foreign Material

    Domino Foods Inc is recalling 50 LB bags of Premium Pure Cane Golden Light Brown Sugar due to possible foreign material.

    Product
    Domino Premium Pure Cane Golden Light Brown Sugar, 50 LB bag, UPC 049200009727, Lots 50041 (Best By Jan 20, 2022), 50042 (Best By Jan 21, 2022), 50043 (Best By Jan 22, 2022)
    Category
    Food
    Distribution
    23 states
  • ModerateFDA (Food)·F-0743-2020·2020-03-04

    Domino Foods Recalls C&H Golden Brown Sugar Due to Foreign Material

    Domino Foods Inc is recalling specific lots of C&H Pure Cane Sugar Golden Brown due to possible foreign material contamination.

    Product
    C&H Pure Cane Sugar Golden Brown, 32 oz (2 LB) plastic bag, UPC 015800090038, Lots 50042 (Best By Jan 21, 2022) & 50043 (Best By Jan 22, 2022)
    Category
    Food
    Distribution
    23 states
  • ModerateFDA (Food)·F-0782-2020·2020-03-04

    Nature's Sunshine SmartMeal Shake Mix Recalled for Unapproved Herbicide

    Pro-Form Manufacturing LLC is recalling Nature's Sunshine SmartMeal Nutritional Shake Mix because the flax seed ingredient contains an unapproved herbicide.

    Product
    Nature's Sunshine SmartMeal Nutritional Shake Mix; Natural Vanilla Flavor Net Wt. 1 lb. 2 oz. (510 g) UPC: 0 99904 03085 5 Product number: 6116-US3085 Distributed by: Nature's Sunshine Products Inc. 1655 North Main Spanish Fork, UT 84660
    Category
    Food
    Distribution
    2 states
  • ModerateFDA (Devices)·Z-1345-2020·2020-03-04

    Philips DigiTrak XT Holter Recorder Software Recall for Malfunction

    Philips is recalling DigiTrak XT Holter Recorders because a software defect causes the device to fail when an AAA battery is present.

    Product
    Philips DigiTrak XT Holter Recorder Software version number B.1 and C.2. The DigiTrak XT Recorder is available in four different configurations. Service tag numbers for these configurations are as follows: - 453564067151 24-Hour Configuration - 453564067161 48-Hour…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0749-2020·2020-03-04

    Domino Foods Recalls SYSCO Light Brown Cane Sugar for Foreign Material

    Domino Foods Inc is recalling specific lots of SYSCO Classic Light Brown Cane Sugar due to possible foreign material. The product was distributed to 23 states and Saudi Arabia.

    Product
    SYSCO Classic Light Brown Cane Sugar, 32 oz (2 LB) plastic bag, UPC 074865755368, Lots 50042 (Best By Jan 21, 2022) & 50051 (Best By Jan 27, 2022)
    Category
    Food
    Distribution
    23 states