The Recall Desk

State

Minnesota product recalls

73,806 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.

Which agencies issued them

These figures cover only the 7,851 recalls whose distribution notice names Minnesota specifically. The 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

41576–41600 of 81657

  • SevereFDA (Devices)·Z-2559-2018·2018-08-08

    Galt Medical Recalls Vascular Dilators and Introducer Kits Due to Endotoxins

    Galt Medical Corporation is recalling specific vascular dilators and introducer kits because they may contain unsafe levels of bacterial endotoxins introduced during manufacturing.

    Product
    1) Vascular Dilator, Sterile EO, Rx Only, Catalog #: DIL-100-12; 2) Dilator, Sterile EO, Rx Only, Catalog #: DIL-600-11; 3) Tearaway Introducer, Sterile EO, Rx Only, Catalog #: a) INT-028-14; b) INT-028-24; c) INT-029-05; d) INT-106-01; e) INT-106-14; 4) Micro-Access…
    Category
    Medical Device
    Distribution
    19 states
  • SevereFDA (Devices)·Z-2558-2018·2018-08-08

    Galt Medical Recalls Sterile Hemostasis Valve Introducer Systems Due to Endotoxins

    Galt Medical Corporation is recalling specific sterile hemostasis valve introducer systems and kits because they may contain unsafe levels of bacterial endotoxins introduced during manufacturing.

    Product
    1) ELITE HV, Hemostasis Valve Introducer System, Sterile EO, Rx Only, Catalog #: a) BCL-100-04; b) BCL-100-05; c) BCL-100-06; d) BCL-500-36; 2) Elite HV Introducer Set, Sterile EO, Rx Only, Catalog #: a) CLI-105-14; 3) AngioGate HV Introducer Kit, Sterile EO, Catalog #…
    Category
    Medical Device
    Distribution
    19 states
  • SevereFDA (Devices)·Z-2563-2018·2018-08-08

    Galt Medical Recalls Centeze Centesis Catheters Due to Bacterial Endotoxins

    Galt Medical Corporation is recalling 300 units of Centeze Centesis Catheters because they may contain unsafe levels of bacterial endotoxins introduced during manufacturing.

    Product
    Centeze Centesis Catheter, Catalog #: a) DRC-006-05, b) DRC-006-15,
    Category
    Medical Device
    Distribution
    19 states
  • SevereFDA (Drugs)·D-1023-2018·2018-08-08

    Pfizer Recalls Daptomycin Injection Due to Microbial Contamination

    Pfizer is recalling Daptomycin for Injection due to reports of adverse events indicative of infusion reactions related to microbiological contamination.

    Product
    Daptomycin for Injection, 500 mg per vial, packaged as 1 Single-dose vial per carton, Rx only, Hospira, Inc., Lake Forest, IL 60045 USA, NDC 0409-0106-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2594-2018·2018-08-08

    Integra LifeSciences Recalls Mayfield Infinity XR2 Base Units Due to Fracture Risk

    Integra LifeSciences is recalling Mayfield Infinity XR2 Low Profile Base Units because the knob assembly in the swivel adapter may fracture or break during use.

    Product
    MAYFIELD INFINITY XR2 LOW PROFILE BASE UNIT, Part Number A2079A The MAYFIELD¿ Infinity XR2 Base Unit is intended to be used to support a patient during diagnostic examination and/or surgical procedures where a rigid support between surgical table and headrest, or skull clamp…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1894-2018·2018-08-08

    Griffith Labs Herb Crouton Seasoning Recalled for Potential Salmonella

    Griffith Labs U.S.A. is recalling 50-pound bags of Herb Crouton Seasoning due to the potential presence of Salmonella from a recalled whey ingredient.

    Product
    Herb Crouton Seasoning 50 pound bag Item 702046300
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2562-2018·2018-08-08

    Galt Medical Elite HV Introducer Recalled for Bacterial Endotoxins

    Galt Medical Corporation is recalling Elite HV Introducers due to potential unsafe levels of bacterial endotoxins introduced during manufacturing.

    Product
    Elite HV Introducer, Catalog #: a) CLI-200-26; b) CLI-210-16; c) CLI-212-07; d) KCL-212-055
    Category
    Medical Device
    Distribution
    19 states
  • HighFDA (Devices)·Z-2602-2018·2018-08-08

    Zimmer Dermatone AN Skin Graft Device Recalled for Loose Control Bar

    Zimmer Surgical Inc is recalling 140 units of the Zimmer Dermatone AN skin graft device due to a loose control bar that may compromise graft thickness control.

    Product
    Zimmer Dermatone AN, Model No. 88710100
    Category
    Medical Device
    Distribution
    17 states
  • HighFDA (Food)·F-1864-2018·2018-08-08

    Griffith Labs Recalls Low Sodium Brown Gravy Mix for Salmonella Risk

    Griffith Labs U.S.A. is recalling Low Sodium Brown Gravy Mix due to the potential presence of Salmonella from a recalled whey ingredient.

    Product
    Low Sodium Brown Gravy Mix 12 oz unit, 8 units per carton Item 860143100 UPC 9624817431
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1869-2018·2018-08-08

    Griffith Labs Recalls Reduced Whey Cold Dough Premix Due to Salmonella Risk

    Griffith Labs U.S.A. is recalling Reduced Whey Cold Dough Premix because it may contain Salmonella from a recalled whey ingredient. The product was distributed nationwide and in Canada.

    Product
    Reduced Whey Cold Dough Premix 2.3 pound bag, 18 units per carton Item 127038500
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1858-2018·2018-08-08

    Griffith Labs Recalls Biscuit Mix Due to Potential Salmonella Risk

    Griffith Labs U.S.A. is recalling specific lots of Biscuit Mix because it may contain Salmonella from a recalled whey ingredient.

    Product
    Biscuit Mix 4.5 pound bag, 8 bags per carton Item 127042301
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1863-2018·2018-08-08

    Griffith Labs Recalls Beef Flavored Gravy Mix Due to Salmonella Risk

    Griffith Labs U.S.A. is recalling Beef Flavored Gravy Mix because it may contain Salmonella from a recalled whey ingredient.

    Product
    Beef Flavored Gravy Mix 12 oz unit, 8 units per carton Item 860143801 UPC 9624817621
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1788-2018·2018-08-08

    General Mills Recalls Cheerios Protein Oats and Honey Cereal

    General Mills is recalling Cheerios Protein Oats and Honey cereal due to potential Salmonella contamination. Consumers should check expiration dates and stop eating the product.

    Product
    Cheerios Protein Oats & Honey, Packaged in the following sizes: Net Wt. 19 oz. (583g) UPC 16000-44473. 12 boxes/case, Net Wt. 14.1 oz. (399g) UPC 16000-45137. 16 boxes/case. Dist. By General M ills Sales, Inc., Minneapolis, MN 55440 USA.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1890-2018·2018-08-08

    Griffith Labs Recalls Country Ranch Crouton Seasoning Due to Salmonella Risk

    Griffith Labs U.S.A. is recalling 50-pound bags of Country Ranch Crouton Seasoning because a whey ingredient used in the product was recalled for potential Salmonella contamination.

    Product
    Country Ranch Crouton Seasoning 50 pound bag Item 859075400
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·18758·2018-08-08

    Polaris Recalls Gravely Utility Vehicles Due to Fire and Burn Hazards

    Polaris is recalling about 2,100 Gravely Atlas JSV 3000 and 6000 utility vehicles because a cracked exhaust header pipe poses fire and burn risks.

    Product
    Gravely Atlas JSV 3000 and 6000 utility vehicles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2578-2018·2018-08-08

    GE Healthcare Recalls CT Systems with Potential UPS Wiring Defect

    GE Healthcare is recalling 42 Discovery IQ 2.0 CT systems installed with a specific electrical panel that may not be properly wired to the uninterruptible power supply.

    Product
    Discovery IQ 2.0 20cm, 4 ring, Model Number 5432539-22
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2472-2018·2018-08-08

    Siemens SOMATOM Emotion 6 CT Scanner Recalled for Radiation Risk

    Siemens Medical Solutions is recalling SOMATOM Emotion 6 CT scanners due to a software issue that may cause unnecessary radiation exposure.

    Product
    SOMATOM Emotion 6 (Model 10165888)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2595-2018·2018-08-08

    Integra LifeSciences Recalls Mayfield Spine Table Adaptors Due to Fracture Risk

    Integra LifeSciences is recalling 95 Mayfield Spine Table Adaptors because the knob assembly may fracture during use, posing a risk to patients.

    Product
    MAYFIELD SPINE TABLE ADAPTOR RADIOLUCENT, Part Number A2600R The MAYFIELD¿ Infinity XR2 Base Unit is intended to be used to support a patient during diagnostic examination and/or surgical procedures where a rigid support between surgical table and headrest, or skull clamp is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2587-2018·2018-08-08

    GE Healthcare Recalls CT Systems with Potential Electrical Wiring Defect

    GE Healthcare is recalling 42 CT and CT/PET systems installed with a specific electrical panel that may not be properly wired to the uninterruptible power supply.

    Product
    CT Goldseal BrightSpeed 16 PWR TIO 2 YR
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1896-2018·2018-08-08

    Griffith Labs Italian Crouton Seasoning Recalled for Potential Salmonella

    Griffith Labs U.S.A. is recalling 555 bags of Italian Crouton Seasoning due to the potential presence of Salmonella from a recalled whey ingredient.

    Product
    Italian Crouton Seasoning 50 pound bag Item 1000017039
    Category
    Food
    Distribution
    Distributed nationwide