The Recall Desk

State

Minnesota product recalls

73,817 recalls have nationwide distribution and so reach Minnesota. 7,851 additional recalls listed Minnesota specifically in their distribution scope.

What the numbers show

Total
7,851
Critical
1,137
Severe
2,246
Most recent
2026-11-04

Of the 7,851 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 2,246 (29%) are Severe.

These figures cover only the 7,851 recalls whose distribution notice names Minnesota specifically. The 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

47201–47225 of 81668

  • HighFDA (Food)·F-2413-2017·2017-07-12

    GoMacro Recalls Specific MacroBars and Thrive Bars Due to Listeria Risk

    GoMacro is recalling specific MacroBars and Thrive Bars because they may be contaminated with Listeria monocytogenes.

    Product
    go macro MACROBAR, coconut + almond butter + chocolate chips, in the following sizes: 1. Net Wt 0.9 oz / 25 G minbar, UPC 8 53555-00671 9 and 2. net Wt 2.3 oz / 65 G, UPC 8 53555-00668 9
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·17185·2017-07-12

    TriggerTech Recalls Crossbow and Rifle Triggers Due to Injury Hazard

    TriggerTech is recalling about 2,000 carbide crossbow and rifle triggers because rollers can crack, causing the weapon to discharge without trigger activation.

    Product
    TriggerTech Carbide crossbow and rifle triggers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2415-2017·2017-07-12

    GoMacro Recalls Thrive Caramel Coconut Bars for Listeria Risk

    GoMacro is recalling specific THRIVE Caramel Coconut bars because they may be contaminated with Listeria monocytogenes.

    Product
    go macro THRIVE Caramel Coconut bar, Net Wt 1.4 oz / 40 G, UPC 8 53555-00652 8
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2685-2017·2017-07-12

    PerkinElmer Multiphor II Electrophoresis System Recalled for Electric Shock Risk

    PerkinElmer is recalling 241 Multiphor II Electrophoresis Systems due to a potential electric shock hazard if grommets are not installed.

    Product
    Multiphor II Electrophoresis System GE HealthCare Product Number: 18-1018-06 PerkinElmer Part Number: 2117-004 Product Usage: Multiphor II Electrophoresis System is a versatile modular electrophoresis system for horizontal electrophoresis, isoelectric focusing, 2-D…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2656-2017·2017-07-12

    JAS Diagnostics Recalls Drew Scientific DREW 3-PAC Reagent Kits

    JAS Diagnostics Inc. is recalling 14,064 units of Drew Scientific DREW 3-PAC Reagent Kits because they may result in elevated platelet backgrounds during routine startup checks.

    Product
    Drew Scientific DREW 3-PAC Reagent Kit containing: 5L Diluent, 750 mL Enzymatic Cleaner, and 125 mL Lysing Reagent.
    Category
    Medical Device
    Distribution
    18 states
  • ModerateFDA (Devices)·Z-2658-2017·2017-07-12

    Encore Medical Recalls 3DKnee Tibial Inserts Due to Mis-packaging Error

    Encore Medical is recalling 9 units of 3DKnee Tibial Inserts because a size 6 left box contained a size 8 right insert.

    Product
    3DKNEE(TM) SYSTEM e+, tibial Insert, LEFT Sz 6 / 11mm, REF 391-11-706, QTY 01, The 3DKnee Insert HXL Tibial Inserts are manufactured from ultra high molecular weight polyethylene (UHMWPE) infused with pure liquid pharmaceutical grade alpha-tocopheral and then cross-linked to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2665-2017·2017-07-12

    Exactech Equinoxe Modular Reverse Pilot-Tip Starter Reamer Recall

    Exactech is recalling 928 Equinoxe Modular Reverse Pilot-Tip Starter Reamers to update instructions for use. The update clarifies proper reaming technique to prevent instrument breakage.

    Product
    EXACTECH Equinoxe Modular Reverse Pilot-Tip Starter Reamer - Catalog #: 321-25-01
    Category
    Medical Device
    Distribution
    33 states
  • ModerateFDA (Devices)·Z-2664-2017·2017-07-12

    Exactech Equinoxe Glenoid Reamer Recalled for Updated Instructions

    Exactech is recalling Equinoxe Glenoid Reamers to update instructions for use, clarifying that off-axis reaming may cause instrument breakage.

    Product
    EXACTECH Equinoxe Glenoid Reamer - Catalog #: 321-05-38, Catalog #: 321-05-42, and Catalog #: 321-05-46
    Category
    Medical Device
    Distribution
    33 states
  • ModerateFDA (Devices)·Z-2668-2017·2017-07-12

    Exactech Equinoxe Reamer Recall Due to Updated Instructions for Use

    Exactech is recalling Equinoxe Narrow Modular Reverse Pilot-Tip Reamers to update instructions for use, clarifying that off-axis reaming may cause instrument breakage.

    Product
    EXACTECH Equinoxe Narrow Modular Reverse Pilot-Tip Reamer // Catalog #: 321-45-38, Catalog #: 321-45-42 and Catalog #: 321-45-46
    Category
    Medical Device
    Distribution
    33 states
  • ModerateFDA (Devices)·Z-2663-2017·2017-07-12

    Exactech Equinoxe Reverse Starter Reamer Recalled for Updated Instructions

    Exactech is recalling 382 Equinoxe Reverse Starter Reamers to update instructions for use, clarifying that off-axis reaming may cause instrument breakage.

    Product
    EXACTECH Equinoxe Reverse Starter Reamer - Catalog #: 321-05-01
    Category
    Medical Device
    Distribution
    33 states
  • ModerateFDA (Devices)·Z-2662-2017·2017-07-12

    Exactech Recalls Logic Fit Tibial Tamp Heads for Labeling Clarification

    Exactech, Inc. is recalling 573 Logic Fit Tibial Tamp Heads to update surgical labeling. The update clarifies proper removal techniques to prevent instrument breakage.

    Product
    Logic Fit Tibial Tamp Head
    Category
    Medical Device
    Distribution
    32 states
  • ModerateFDA (Drugs)·D-0945-2017·2017-07-12

    G & W Clobetasol Propionate Ointment Recalled for Impurity

    G & W Laboratories is recalling Clobetasol Propionate Ointment 0.05% due to out-of-specification results for a known impurity.

    Product
    CLOBETASOL PROPIONATE — CLOBETASOL PROPIONATE (CLOBETASOL PROPIONATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0937-2017·2017-07-12

    Methocarbamol USP Recalled for Quality Assurance Deviations

    American Pharmaceutical Ingredients LLC is recalling Methocarbamol USP due to lack of quality assurance at the API manufacturer.

    Product
    Methocarbamol, USP, packaged in a) 100 g container (NDC: 58597-8023-6, b) 500 g container (NDC: 58597-8023-7), c) 1,000 g container (NDC: 58597-8023-8). For Prescription Compounding RX Only. Packed under cGMP conditions by American Pharmaceutical Ingredients, LLC 6650 Highland…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2423-2017·2017-07-12

    Nutri-Dyn Calcium D-Glucarate Plus Recalled Due to Mislabeling

    Nutri-Dyn Midwest, Inc. is recalling 856 bottles of Calcium D-Glucarate Plus because they were mistakenly labeled as St. John's Wort during production.

    Product
    Nutri-Dyn Calcium D-Glucarate Plus, Dietary Supplement, 60 Capsules, UPC 7 13757-09611 9
    Category
    Food
    Distribution
    24 states
  • ModerateFDA (Devices)·Z-2666-2017·2017-07-12

    Exactech Equinoxe Modular Reverse Pilot-Tip Reamer Recall for Labeling Clarification

    Exactech is recalling Equinoxe Modular Reverse Pilot-Tip Reamers to update instructions for use, clarifying that off-axis reaming may cause instrument breakage.

    Product
    EXACTECH Equinoxe Modular Reverse Pilot-Tip Reamer, Catalog #: 321-25-38, Catalog #: 321-25-42 and Catalog #: 321-25-46
    Category
    Medical Device
    Distribution
    33 states
  • ModerateFDA (Drugs)·D-0944-2017·2017-07-12

    GSK Recalls Parodontax Toothpaste Due to Possible Metal Presence

    GSK Consumer Healthcare is recalling 15,708 tubes of Parodontax Whitening toothpaste due to the possibility of metal in the product.

    Product
    PARODONTAX — PARODONTAX (STANNOUS FLUORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0934-2017·2017-07-12

    PharMEDium Recalls Ropivacaine HCl Injection Due to Labeling Errors

    PharMEDium Services, LLC is recalling 21 pumps of Ropivacaine HCl 0.2% injection due to incorrect or missing lot and expiration dates.

    Product
    Ropivacaine HCl 0.2% 550 mL Total Volume in an AutoFuser Pump in 0.9% Sodium Chloride Injection, Rx Only, Compounded by PharMEDium Services, LLC, Sugar Land, TX 77478, NDC: 61553-100-13
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0935-2017·2017-07-12

    PharMEDium Recalls Bupivacaine Pumps Due to Incorrect Labeling

    PharMEDium Services is recalling two Bupivacaine HCl ON-Q pumps due to incorrect or missing lot and expiration date labeling.

    Product
    Bupivacaine HCl 0.25% 270 mL Total Volume in an ON-Q Pump in 0.9% Sodium Chloride Injection in 270 mL, Rx Only, Compounded by PharMEDium Services, LLC, Sugar Land, TX 77478, NDC: 61553-044-57
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2659-2017·2017-07-12

    Encore Medical Recalls 3DKnee Tibial Inserts Due to Mis-Packaging

    Encore Medical is recalling 3DKnee Tibial Inserts because a size 6 left box contained a size 8 right insert.

    Product
    3DKNEE(TM) SYSTEM e+, Tibial Insert, RIGHT Sz 8 / 11mm, REF 391-11-708, QTY 01 The 3DKnee Insert HXL Tibial Inserts are manufactured from ultra high molecular weight polyethylene (UHMWPE) infused with pure liquid pharmaceutical grade alpha-tocopheral and then cross-linked to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0932-2017·2017-07-12

    PharMEDium Recalls Ropivacaine Pumps Due to Labeling Errors

    PharMEDium Services is recalling 147 Ropivacaine HCl IV pumps nationwide because of incorrect or missing lot and expiration dates.

    Product
    Ropivacaine HCl 0.2% 500 mL Total Volume in an ON-Q Pump in 0.9% Sodium Chloride Injection in 400 mL, Rx Only, Compounded by PharMEDium Services, LLC, Sugar Land, TX 77478, NDC: 61553-258-25
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0930-2017·2017-07-12

    PharMEDium Recalls Ropivacaine Pumps Due to Incorrect Labeling

    PharMEDium Services is recalling 79 Ropivacaine HCl IV pumps because of incorrect or missing lot and expiration dates.

    Product
    Ropivacaine HCl 0.2% 400 mL Total Volume in an ON-Q Pump in 0.9% Sodium Chloride Injection in 400 mL, Rx Only, Compounded by PharMEDium Services, LLC, Sugar Land, TX 77478, NDC: 61553-256-09
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0936-2017·2017-07-12

    PharMEDium Recalls Bupivacaine Pumps Due to Incorrect Labeling

    PharMEDium Services is recalling seven Bupivacaine HCl ON-Q pumps because of incorrect or missing lot and expiration dates.

    Product
    Bupivacaine HCl 0.25% 400 mL Total Volume in an ON-Q Pump in 0.9% Sodium Chloride Injection in 400 mL, Rx Only, Compounded by PharMEDium Services, LLC, Sugar Land, TX 77478, NDC: 61553-023-09
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0931-2017·2017-07-12

    PharMEDium Recalls Ropivacaine Pumps Due to Labeling Errors

    PharMEDium Services is recalling 22 Ropivacaine HCl pumps nationwide because of incorrect or missing lot and expiration dates.

    Product
    Ropivacaine HCl 0.2% 500 mL Total Volume in an ON-Q Pump in 0.9% Sodium Chloride Injection in 400 mL, Rx Only, Compounded by PharMEDium Services, LLC, Sugar Land, TX 77478, NDC: 61553-258-03
    Category
    Drug
    Distribution
    Distributed nationwide