The Recall Desk

State

Minnesota product recalls

73,824 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 73,824 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

51826–51850 of 81675

  • HighFDA (Devices)·Z-2909-2016·2016-10-12

    Integra Ventricular Catheter Accessory Kit Recalled for Incomplete Packaging Seal

    Integra LifeSciences Corp. is recalling 14 units of the Ventricular Catheter Accessory Kit due to an incomplete sterile packaging seal discovered during final inspection.

    Product
    Integra Ventricular Catheter Accessory Kit, REF 951303, Sterile EO, Rx only, packaged in a PVC tray, then secondary package in to Tyvek pouch and tertiary packaged in to Tyvek pouch. Sealed pouches are packaged in a cardboard box. F8 35cm Silicone Elastomer Ventricular…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0039-2017·2016-10-12

    Siemens Dimension Vista Calcium Reagent Cartridge Recall for Erroneous Results

    Siemens Healthcare Diagnostics is recalling Dimension Vista Calcium reagent cartridges that may produce inaccurate test results.

    Product
    Dimension Vista¿ Calcium (CA) Flex¿ reagent cartridge Device Listing No.: D011443 Batch Number: 16060BB
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0014-2017·2016-10-12

    Siemens Recalls Multix Fusion VA10 Radiographic Systems Due to Table Defect

    Siemens is recalling 37 Multix Fusion VA10 radiographic systems because a table part may detach, causing the table to tilt and potentially injure patients.

    Product
    Multix Fusion VA10 Product Usage: The Multix Fusion VA10 system is a radiographic system used in hospitals, clinics, and medical practices. Multix Fusion enables radiographic exposures of the whole body including:skull, chest, abdomen and extremities and may be used on…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0008-2017·2016-10-12

    Microgenics Recalls QMS Everolimus Assay Due to Reagent Stability Issue

    Microgenics Corporation is recalling the Thermo Scientific QMS Everolimus Assay because a reagent stability issue causes inaccurate test results for transplant patients.

    Product
    Thermo Scientific QMS Everolimus Assay; Model number: 0380000 (US Distribution); 0373852 (Foreign Distribution) Product Usage: The QMS Everolimus Assay is intended for the quantitative determination of Everolimus, in human whole blood on automated clinical chemistry…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0003-2017·2016-10-12

    Zimmer Biomet Recalls Vanguard 360 Knee Prostheses Due to Bolt Defect

    Zimmer Biomet is recalling 454 Vanguard 360 Revision Knee System prostheses because a manufacturing defect in the tibial augment bolts may prevent them from being fully tightened during surgery.

    Product
    Vanguard 360 Revision Knee System Knee prostheses
    Category
    Medical Device
    Distribution
    9 states
  • HighCPSC·17010·2016-10-12

    Mamas & Papas Recalls Armadillo Strollers Due to Fall Hazard

    Mamas & Papas is recalling Armadillo Flip and Flip XT strollers because a loose latch can cause the seat to tip back, posing a fall hazard to infants.

    Product
    Mamas & Papas Armadillo Flip Strollers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V728000·2016-10-12

    Forest River Recalls 2017 Trailers Due to Air Conditioner Fire Risk

    Forest River is recalling 2017 Flagstaff and Rockwood trailers because excess slack in air conditioner wiring may contact heating elements, increasing fire risk.

    Product
    FOREST RIVER — FOREST RIVER ROCKWOOD, FLAGSTAFF
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0016-2017·2016-10-12

    Panoramic PC-1000 X-ray Systems Recalled for Safety Nut Defect

    Panoramic Rental Corp. is voluntarily correcting PC-1000 X-ray systems because a safety nut may be ineffective, posing a risk of blunt force trauma to the head, neck, or shoulders.

    Product
    Panoramic X-ray Model PC-1000, Laser-1000 packed in a crate Product Usage: The PC-1000 will enable the user to take panoramic x-ray images. The PC-1000/Laser1000 will enable the user to take panoramic x-ray images as well as cephalometric x-ray images.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·16V727000·2016-10-12

    Keystone Recalls 2017 Dutchmen Coleman Trailers for Wiring Fire Risk

    Keystone RV is recalling 84 model year 2017 Dutchmen Coleman recreational trailers because loose or frayed wiring in the power center may increase the risk of a fire.

    Product
    DUTCHMEN — DUTCHMEN COLEMAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0005-2017·2016-10-12

    Teva Recalls Claravis Isotretinoin Capsules Due to Impurity Failures

    Teva North America is recalling Claravis (isotretinoin) capsules because they failed impurity and degradation specifications.

    Product
    Claravis (isotretinoin capsules USP), 10mg, packaged in carton containing 3 Blister Packs of 10 Capsules Each (30 Capsules total); Rx only, TEVA PHARMACEUTICALS USA, Sellersville, PA 18960. NDC 00555-1054-86
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0024-2017·2016-10-12

    Ivoclar Vivadent Recalls Zenostar MT Color A3.5 Dental Porcelain Coloring Liquid

    Ivoclar Vivadent is recalling 17 units of Zenostar MT Color A3.5 dental porcelain coloring liquid due to potential packaging leaks that may cause skin irritation.

    Product
    Zenostar MT Color A3.5 60ml, art. no. 681053. Product Usage: For coloring dental porcelain
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0047-2017·2016-10-12

    Toshiba Aquilion RXL CT Scanner Recalled for Reconstruction Error

    Toshiba is recalling 165 Aquilion RXL CT scanners because a reconstruction error may interrupt scans if the range exceeds the maximum field of view.

    Product
    Toshiba America Medical Systems, Inc . Aquilion RXL TSX-101 A/R, U CT Scanner Diagnostic imaging systems indicated to acquire and display cross sectional volumes of the whole body, to include the head.
    Category
    Medical Device
    Distribution
    35 states
  • ModerateFDA (Devices)·Z-2906-2016·2016-10-12

    Integra CUSA Dissectron Fingertip Laparoscopic Cannula Recalled for Packaging Seal Defect

    Integra LifeSciences is recalling 9 units of CUSA Dissectron Fingertip Laparoscopic Cannulas due to incomplete sterile packaging seals discovered during final inspection.

    Product
    CUSA Dissectron Fingertip Laparoscopic Cannula, REF F75221, Sterile EO, Rx only, packaged in a Tyvek pouch and secondary packaged in Tyvek pouch, Five (5) sealed pouches are packaged in a cardboard box. For use with CUSA DISSECTRON Hand pieces and Sontrodes
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0018-2017·2016-10-12

    Ivoclar Vivadent Recalls Zenostar MT Color Impulse Brown Dental Porcelain

    Ivoclar Vivadent is recalling 11 units of Zenostar MT Color Impulse brown dental porcelain due to potential packaging leaks that may cause skin irritation.

    Product
    Zenostar MT Color Impulse brown, art. no. 681169 Product Usage: For coloring dental porcelain
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0012-2017·2016-10-12

    Philips Ingenuity CT Scanner Recalled for Infant Head Image Quality Issues

    Philips Medical Systems is recalling 235 Ingenuity CT scanners because infant head scans in High Resolution mode may produce degraded image quality, including non-uniformity and CT number shifts.

    Product
    Ingenuity CT Model Number 728326 Product Usage: Computed Tomography X-ray systems intended to product 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-0017-2017·2016-10-12

    Ivoclar Vivadent Recalls Zenostar MT Color Impulse Blue Dental Porcelain

    Ivoclar Vivadent is recalling 79 units of Zenostar MT Color Impulse blue dental porcelain due to packaging leaks that may cause skin irritation.

    Product
    Zenostar MT Color Impulse blue, Art. no. 681165 Product Usage: For coloring dental porcelain
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0032-2017·2016-10-12

    Ivoclar Vivadent Recalls Zenostar MT Color C3 Dental Porcelain Coloring Liquid

    Ivoclar Vivadent is recalling 13 units of Zenostar MT Color C3 dental porcelain coloring liquid due to packaging leaks that may cause skin irritation.

    Product
    Zenostar MT Color C3 60ml, art. no. 681061. Product Usage: For coloring dental porcelain
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0049-2017·2016-10-12

    Toshiba Celesteion CT Scanner Recalled for Potential Reconstruction Errors

    Toshiba is recalling 165 Celesteion CT scanners because a reconstruction error may interrupt scanning if the scan range exceeds the maximum field of view.

    Product
    Toshiba America Medical Systems, Inc . Celesteion PCA-9000A/2 CT Scanner
    Category
    Medical Device
    Distribution
    35 states
  • ModerateFDA (Devices)·Z-0028-2017·2016-10-12

    Ivoclar Vivadent Recalls Zenostar MT Color B3 Dental Porcelain Liquid

    Ivoclar Vivadent is recalling 27 units of Zenostar MT Color B3 dental porcelain liquid due to potential packaging leaks that may cause skin irritation.

    Product
    Zenostar MT Color B3 60ml, art. no. 681057. Product Usage: For coloring dental porcelain
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0048-2017·2016-10-12

    Toshiba Aquilion LB CT Scanner Recalled for Reconstruction Error

    Toshiba is recalling 165 Aquilion LB CT scanners because a reconstruction error may interrupt scanning if the range exceeds the maximum field of view.

    Product
    Toshiba America Medical Systems, Inc . Aquilion LB TSX-201A/2, 3 CT Scanner
    Category
    Medical Device
    Distribution
    35 states
  • ModerateFDA (Devices)·Z-0027-2017·2016-10-12

    Ivoclar Vivadent Recalls Zenostar MT Color B2 Dental Porcelain Coloring Liquid

    Ivoclar Vivadent is recalling 15 units of Zenostar MT Color B2 dental porcelain coloring liquid due to packaging leaks that may cause skin irritation.

    Product
    Zenostar MT Color B2 60ml, art. no. 681056. Product Usage: For coloring dental porcelain
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0026-2017·2016-10-12

    Ivoclar Vivadent Recalls Zenostar MT Color B1 Dental Porcelain Coloring Liquid

    Ivoclar Vivadent is recalling 43 units of Zenostar MT Color B1 dental porcelain coloring liquid due to packaging leaks that may cause skin irritation.

    Product
    Zenostar MT Color B1 60ml, art. no. 681055. Product Usage: For coloring dental porcelain
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0035-2017·2016-10-12

    Ivoclar Vivadent Recalls Zenostar MT Color D3 Dental Porcelain Coloring Liquid

    Ivoclar Vivadent is recalling 18 units of Zenostar MT Color D3 dental porcelain coloring liquid due to packaging leaks that may cause skin irritation.

    Product
    Zenostar MT Color D3 60ml, art. no. 681064. Product Usage: For coloring dental porcelain
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0036-2017·2016-10-12

    Ivoclar Vivadent Recalls Zenostar MT Color D4 Dental Porcelain Coloring Liquid

    Ivoclar Vivadent is recalling 9 units of Zenostar MT Color D4 dental porcelain coloring liquid due to packaging leaks that may cause skin irritation.

    Product
    Zenostar MT Color D4 60ml, art. no. 681065. Product Usage: For coloring dental porcelain
    Category
    Medical Device
    Distribution
    Distributed nationwide