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.

Which agencies issued them

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.

48701–48725 of 81668

  • ModerateFDA (Drugs)·D-0665-2017·2017-04-19

    Medisca Recalls Estradiol API Due to cGMP Deviations

    Medisca, Inc. is recalling Estradiol, USP (Hemihydrate) (Micronized) API products due to cGMP deviations identified during a recent FDA inspection.

    Product
    ESTRADIOL, USP (Hemihydrate)(Micronized), in a) 100 mg (NDC 38779-0869-07), b) 1 g (NDC 38779-0869-06), c) 5 g (NDC 38779-0869-03), d) 10 g (NDC 38779-0869-01), e) 25 g (NDC 38779-0869-04), f) 100 g (NDC 38779-0869-05) , g) 500 g (NDC 38779-0869-08), h) 1 Kg (NDC 38779-0869-09)…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1810-2017·2017-04-19

    FDA Recalls Volt Heated Slippers for Unapproved Medical Claims

    2k Innovations Inc. is recalling Volt Resistance Heated Slippers because FDA inspections found the product makes unapproved therapy and medical claims.

    Product
    Volt Resistance Heated Slipper Black (All sizes) Deep penetrating heat garment and wraps
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1812-2017·2017-04-19

    FDA Recalls Volt Heated Slippers for Unapproved Medical Claims

    2k Innovations Inc. is recalling Volt Resistance Heated Slippers because the firm made unapproved therapy and medical claims on product information and its website.

    Product
    Volt Resistance Heated Slipper (All sizes) Deep penetrating heat garment and wraps
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1806-2017·2017-04-19

    FDA Recalls Volt Heated Knee Wrap for Unapproved Medical Claims

    2k Innovations Inc. is recalling Volt Resistance Heated Therapy Knee Wraps because FDA inspections found the product makes unapproved therapy and medical claims.

    Product
    Volt Resistance Heated Therapy Knee Wrap Deep penetrating heat garment and wraps
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1797-2017·2017-04-19

    Windstone Medical Recalls PRK Trays Due to Sterile Packaging Concerns

    Windstone Medical Packaging is recalling 20 PRK kits because the sterile packaging of the included eye pads may be compromised.

    Product
    PRK Tray, part number DDS1044 Product packaged in a convenient manner for use in a general clinical procedure
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1818-2017·2017-04-19

    Keystone Dental Recalls PrimaConnex Straight Implants Due to Mislabeling

    Keystone Dental Inc. is recalling 59 PrimaConnex Straight Implants because they were incorrectly labeled as Tapered Implants.

    Product
    Keystone Dental Inc. PrimaConnex Straight Implant TC, WD Internal Connection 5.0 x 11.5mm. Catalog Number(s): 15636K
    Category
    Medical Device
    Distribution
    9 states
  • ModerateFDA (Devices)·Z-1813-2017·2017-04-19

    FDA Recalls Heated Slippers for Unapproved Medical Claims

    2k Innovations Inc. is recalling Volt Resistance Unisex Rechargeable Heated Slippers because FDA inspections found the company made unapproved therapy and medical claims.

    Product
    Volt Resistance Unisex Rechargeable Heated Slipper (All sizes) Deep penetrating heat garment and wraps
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1789-2017·2017-04-19

    Windstone ENT Pack Recall Due to Compromised Sterile Packaging

    Windstone Medical Packaging is recalling 16 ENT kits because the sterile packaging of the included Medtronic eye pads may be compromised.

    Product
    ENT Pack, part number AMS2727 Product packaged in a convenient manner for use in a general clinical procedure
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0656-2017·2017-04-19

    FDA Recalls Estriol Micronized Bulk Drug Due to Quality Assurance Failures

    Qinhuangdao Zizhu Pharmaceutical is recalling bulk Estriol Micronized, USP, due to cGMP deviations and lack of quality assurance. The product is distributed to pharmacies in six states for prescription compounding.

    Product
    Estriol Micronized, USP, Bulk, Rx only, For Prescription Compounding, Manufactured by Qinhuangdao Zizhu Pharmaceutical Co., Ltd, Qinhuangdao 066004, China 44132-007-06
    Category
    Drug
    Distribution
    6 states
  • LowFDA (Drugs)·D-0671-2017·2017-04-19

    Jubilant Cadista Recalls Bupropion Hydrochloride Tablets for Impurity Failure

    Jubilant Cadista Pharmaceuticals is recalling Bupropion Hydrochloride Extended-release Tablets because high levels of a degradation product were detected.

    Product
    BuPROPion Hydrochloride Extended-release Tablets, USP (SR), 200 mg, packaged in a) 60-count bottles (NDC 59746-317-60) and b) 100-count bottles (NDC 59746-317-01), Rx only, Manufactured by: Julibant Life Sciences Ltd., Roorkee-247661, India; Marketed by: Jubilant Cadista…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1767-2017·2017-04-19

    Smiths Medical CADD Administration Set Recalled for Incorrect Filter Size Illustration

    Smiths Medical is recalling CADD Administration Sets because the illustration on the Instructions for Use incorrectly depicts the filter size as 2.0 microns instead of the actual 0.2 microns.

    Product
    CADD¿ Administration Set, 21-7339-24, Rx Only, Sterile EO.
    Category
    Medical Device
    Distribution
    43 states
  • LowFDA (Drugs)·D-0669-2017·2017-04-19

    Jubilant Cadista Recalls Bupropion Hydrochloride Tablets for Impurity Issues

    Jubilant Cadista Pharmaceuticals is recalling specific lots of Bupropion Hydrochloride Extended-release Tablets due to high levels of a degradation product.

    Product
    BuPROPion Hydrochloride Extended-release Tablets, USP (SR), 100 mg, packaged in a) 60-count bottles (NDC 59746-315-60) and b) 100-count bottles (NDC 59746-315-01), Rx only, Manufactured by: Julibant Life Sciences Ltd., Roorkee-247661, India; Marketed by: Jubilant Cadista…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·17E021000·2017-04-18

    Cummins Recalls ISV5.0 Diesel Engines in Tiffin Breeze Motorhomes

    Cummins is recalling ISV5.0 diesel engines in Tiffin Breeze motorhomes because a fan support bearing may fail, causing the engine to stall and increasing crash risk.

    Product
    ENGINE AND ENGINE COOLING:ENGINE:DIESEL recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V255000·2017-04-18

    Micro Bird Recalls MB II School Buses for Roof Crush Risk

    Micro Bird is recalling 2012-2017 MB II school buses because the roof may crush during a rollover, increasing injury risk.

    Product
    MICRO BIRD — MICRO BIRD MB II SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V258000·2017-04-18

    Volvo Recalls 2015-2017 VHD Trucks for Incorrect Axle Weight Labels

    Volvo is recalling 2015-2017 VHD trucks because the Gross Axle Weight Rating on the certification label may be incorrect, which could lead to vehicle overloading.

    Product
    VOLVO — VOLVO VHD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·17V256000·2017-04-18

    Honda Recalls 2017 CR-V and Acura RDX for Fading Certification Labels

    Honda is recalling 2017 CR-V and Acura RDX vehicles because certification labels may wipe away with alcohol solvents, potentially leading to vehicle overload.

    Product
    ACURA — ACURA, HONDA RDX, CR-V
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17E020000·2017-04-13

    FiveCubits Recalls TREQ-VMx Tablets Due to Battery Overheating Risk

    FiveCubits is recalling TREQ-VMx mobile data tablets used by commercial truck operators because the lithium ion polymer batteries may overheat, increasing the risk of fire.

    Product
    ELECTRICAL SYSTEM:SOFTWARE recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V253000·2017-04-13

    Nissan Recalls Sentra and Leaf Vehicles for Air Bag Defect

    Nissan is recalling 2014-2017 Sentra and 2015-2017 Leaf vehicles because the front passenger air bag may not deploy properly in a crash.

    Product
    NISSAN — NISSAN SENTRA, LEAF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17132·2017-04-13

    Polaris Recalls Ranger 900 Vehicles Due to Fire and Burn Hazards

    Polaris is recalling about 51,000 Ranger 900 recreational off-highway vehicles because a heat shield can fall off, posing fire and burn hazards.

    Product
    Polaris Ranger 900 recreational off-highway vehicles (ROVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide