The Recall Desk

State

Minnesota product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

54076–54100 of 81678

  • ModerateFDA (Devices)·Z-1838-2016·2016-06-08

    Baxter Recalls COSEAL Surgical Sealant Kits Due to Dissolution Issues

    Baxter Healthcare is recalling 274 units of COSEAL Surgical Sealant Kits because the PEG component may not fully dissolve, affecting hydrogel consistency.

    Product
    COSEAL Surgical Sealant Kit, 2 mL, Product Code: 934070; For use in vascular reconstructions to achieve adjunctive hemostasis by mechanically sealing areas of leakage.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1843-2016·2016-06-08

    Medscience AllergiEnd Skin Test Applicators Recalled for Lack of Clearance

    Medscience Inc is recalling AllergiEnd ST-9 skin test applicators and trays because they were marketed without FDA clearance.

    Product
    AllergiEnd ST-9 Multiple Skin Test Applicator (Item 1000) and AllergiEnd ST-9 Multiple Well Test Tray (Item (1001). Contents: 8 applicators to perform up to 72 skin tests. Perform a multi-site skin test to identify reactions to certain allergens using a non-invasive applicator…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1874-2016·2016-06-08

    Philips Ingenuity Core 128 CT Systems Recalled for Drive Mapping Issue

    Philips Medical Systems is recalling 424 Ingenuity Core 128 CT systems because the system may not map the Varian drive after a user logout and login.

    Product
    Ingenuity Core 128 Computed Tomography X-ray Systems Product Usage: Intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1875-2016·2016-06-08

    Philips Ingenuity CT Systems Recalled for Drive Mapping Issue

    Philips is recalling 215 Ingenuity CT systems because they may fail to map the Varian drive after a user logs out and back in.

    Product
    Ingenuity Computed Tomography X-ray Systems Product Usage: Intended to produce cross-sectional images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1839-2016·2016-06-08

    Baxter Recalls COSEAL Surgical Sealant Kits Due to Dissolution Issues

    Baxter Healthcare is recalling 6,804 units of COSEAL Surgical Sealant Kits because the PEG component may not fully dissolve, affecting hydrogel consistency.

    Product
    COSEAL Surgical Sealant Kit, 4 mL, Product Code: 934071; For use in vascular reconstructions to achieve adjunctive hemostasis by mechanically sealing areas of leakage.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0954-2016·2016-06-08

    Lupin Recalls Ceftriaxone Injection Vials Due to CGMP Deviations

    Lupin Pharmaceuticals is recalling 570 vials of Ceftriaxone for Injection USP, 2 g, because the active pharmaceutical ingredients used in manufacturing failed specifications.

    Product
    Ceftriaxone for Injection USP, 2 g, Single Use Vial (NDC 68180-644-01) packaged in 10-count Vials per box (NDC 68180-644-10), Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., 111 South Calvert Street, Baltimore, Maryland 21202; Manufactured by: Lupin Limited, Mandideep…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0953-2016·2016-06-08

    Lupin Recalls Ceftriaxone Injection Vials Due to CGMP Deviations

    Lupin Pharmaceuticals is recalling Ceftriaxone for Injection vials because they were manufactured using active pharmaceutical ingredients that failed specifications.

    Product
    Ceftriaxone for Injection USP, 1 g, Single Use Vial (NDC 68180-633-01) packaged in 10-count Vials per box (NDC 68180-633-10), Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., 111 South Calvert Street, Baltimore, Maryland 21202; Manufactured by: Lupin Limited, Mandideep…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0952-2016·2016-06-08

    Lupin Recalls Ceftriaxone Injection Vials Due to CGMP Deviations

    Lupin Pharmaceuticals is recalling Ceftriaxone for Injection USP, 500 mg, because the active ingredients used in manufacturing failed specifications.

    Product
    Ceftriaxone for Injection USP, 500 mg, Single Use Vial, packaged in a) 1-count Vials per box (NDC 68180-622-01), and b) 10-count Vials per box (NDC 68180-622-10), Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., 111 South Calvert Street, Baltimore, Maryland 21202…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0951-2016·2016-06-08

    Lupin Recalls Ceftriaxone Injection Vials Due to CGMP Deviations

    Lupin Pharmaceuticals is recalling specific lots of Ceftriaxone for Injection USP because they were manufactured using active pharmaceutical ingredients that failed specifications.

    Product
    Ceftriaxone for Injection USP, 250 mg, Single Use Vial, packaged in a) 1-count Vials per box (NDC 68180-611-01), and b) 10-count Vials per box (NDC 68180-611-10), Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., 111 South Calvert Street, Baltimore, Maryland 21202…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1909-2016·2016-06-08

    Affymetrix Recalls CytoScan Dx Assay Kits Due to Missing Warning Statements

    Affymetrix is recalling 507 CytoScan Dx Assay kits because FDA inspectors found that required warning statements were missing from product shipments.

    Product
    CytoScan¿ Dx Assay. The CytoScan Dx Assay consists of five reagent modules, wash buffers (WS), a microarray kit, and analysis software. The CytoScan Dx Assay consists of five reagent modules, wash buffers (WS), a microarray kit, and analysis software: MOD R LA, CytoScan¿ Dx…
    Category
    Medical Device
    Distribution
    15 states
  • LowFDA (Devices)·Z-1907-2016·2016-06-08

    B. Braun Recalls Non-Vented Dispensing Pins Due to Packaging Tears

    B. Braun Medical is recalling 11,000 Non-Vented Dispensing Pins because the outer blister packaging may tear, potentially compromising the device.

    Product
    Non-Vented Dispensing Pin with Luer Lock Ultrasite Valve Product Usage: Used for aspiration of medication from inverted bags or semi-rigid containers. Interavenous delivery of transferred medication(Device is not intended for direct infusion)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0955-2016·2016-06-08

    Lupin Recalls Ceftriaxone Sodium API Due to CGMP Deviations

    Lupin Pharmaceuticals Inc. is recalling Ceftriaxone Sodium (Sterile) USP active pharmaceutical ingredient because intermediates failed specifications.

    Product
    Ceftriaxone Sodium (Sterile) USP active pharmaceutical ingredient, DMF No. 15931; Manufactured by: Lupin Limited, Unit-1, 198-202, New Industrial Area No. 2, Dist. Raisen, Mandideep-462 046, (Madhya Pradesh) India; Regd. Office: 159, CST Road Kalina, Santacruz (E), Mumbai- 400…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1906-2016·2016-06-08

    B. Braun Medical Recalls Non-Vented Dispensing Pins Due to Packaging Tears

    B. Braun Medical is recalling approximately 11,000 Non-Vented Dispensing Pins because the outer blister packaging may tear, potentially compromising the product label.

    Product
    Non-Vented Dispensing Pin with One-Way Valve and Luer Lock Ultrasite Valve Product Usage: Used for aspiration of medication from inverted bags or semi-rigid containers. Interavenous delivery of transferred medication(Device is not intended for direct infusion)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·16752·2016-06-07

    Focus Bicycles Recalls Spine Models Due to Frame Collapse Risk

    Focus Bicycles is recalling about 80 Spine mountain bicycles because incorrectly sized seatstay or linkage parts can cause the frame to collapse, posing a fall hazard.

    Product
    Focus Spine bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V407000·2016-06-07

    Thomas Built Buses Recall Emergency Door Handle Corrosion Defect

    Daimler Trucks North America is recalling 717 Thomas Built Buses because corrosion on the emergency door handle stem could delay evacuation during an emergency.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES, THOMAS SAF-T-LINER MVP-EF, SAF-T-LINER ER, CL-960, VISTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V404000·2016-06-06

    Lakota Recalls 2016 Trailers Due to Aluminum Rim Pin Holes

    Lakota is recalling 2016 Bighorn, Charger, and Livestock Edition trailers because pin holes in aluminum rims may cause tire failure and increase crash risk.

    Product
    LAKOTA — LAKOTA BIGHORN, LIVESTOCK EDITION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16E052000·2016-06-06

    Meritor Recalls Front Axles Due to Potential Heat Treatment Defect

    Meritor is recalling specific FF967 Non-Drive Front Steer axles manufactured in 2012 because they may have been incorrectly heat treated, posing a risk of fracture and loss of vehicle control.

    Product
    SUSPENSION:FRONT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V403000·2016-06-06

    Volkswagen Recalls 2016 Jetta, Passat, and Golf for Fuel Rail Defect

    Volkswagen is recalling specific 2016 Jetta, Passat, and Golf vehicles because the fuel rail may detach, causing a fuel leak that could lead to a vehicle fire.

    Product
    VOLKSWAGEN — VOLKSWAGEN GOLF, JETTA, PASSAT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V405000·2016-06-06

    Blue Bird Recalls Transit Buses with Defective Wheelchair Lifts

    Blue Bird is recalling 2015-2017 All American and 2016-2017 Vision transit buses equipped with Ricon S-Series wheelchair lifts due to potential platform cracking and bearing displacement.

    Product
    BLUE BIRD — BLUE BIRD VISION, ALL AMERICAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·047-2016·2016-06-04

    Solomon Snacks Recalls Meat Pies for Undeclared Allergens and Lack of Inspection

    Solomon Snacks and Bakery is recalling approximately 873 pounds of meat pies produced without federal inspection and containing undeclared eggs, milk, and wheat.

    Product
    Solomon Snacks and Bakery Recalls Meat Pie Products Produced Without Benefit of Inspection and Due To Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    2 states
  • HighNHTSA·16V401000·2016-06-03

    Chrysler Sebring and Dodge Stratus Recall for Sun Visor Tether Defect

    Mitsubishi is recalling 2001-2002 Chrysler Sebring and Dodge Stratus vehicles with beige interiors because an incorrect part may allow the passenger sun visor to detach during airbag deployment.

    Product
    CHRYSLER — CHRYSLER, DODGE SEBRING, STRATUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V400000·2016-06-03

    Spartan Gladiator and MetroStar Emergency Vehicles Recalled for Pump Defect

    Spartan is recalling 2015 Gladiator and MetroStar emergency vehicles because improperly soldered pump strainers may break, potentially damaging the pump and reducing firefighting effectiveness.

    Product
    SPARTAN — SPARTAN GLADIATOR, METROSTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·16751·2016-06-02

    Hillsdale Furniture Recalls Children's Bunk Beds Due to Fall Hazard

    Hillsdale Furniture is recalling about 20,000 children's bunk beds sold at Bob's Discount Furniture because support rails can crack or break, posing a fall hazard.

    Product
    Children's bunk beds
    Category
    Consumer Product
    Distribution
    Distributed nationwide