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.

51226–51250 of 81675

  • SevereFDA (Devices)·Z-0180-2017·2016-10-26

    Windstone Medical Packaging Recalls Endoscopy Packs Due to Sterility Concerns

    Windstone Medical Packaging is recalling 304 Endoscopy Packs because disposable gloves in the kits may have splits or holes that compromise sterility.

    Product
    Endoscopy Pack, Kit number PSS1646 convenience custom kits used for general surgery in hospital operating room
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0290-2017·2016-10-26

    RTI Surgical Recalls Streamline OCT Spinal Rods Due to Cracks

    RTI Surgical is voluntarily recalling 66 units of Streamline OCT spinal rods due to potential cracks that could reduce strength and cause patient injury.

    Product
    RTI Surgical Streamline OCT Occipito-Cervico-Thoracic Spinal Rod, CoCr, 3.2mm (D) x 240mm (L) Product Usage: When intended to promote fusion of the cervical spine and occipitocervico-thoracic junction (occiput-T3), the Streamline OCT Occipito-Cervico-Thoracic System is…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0193-2017·2016-10-26

    QualiTech Recalls FE Bacon 286 Due to Potential E. coli O121 Presence

    QualiTech is recalling 400 lbs of FE Bacon 286 because a supplier reported the potential presence of E. coli O121 bacteria.

    Product
    FE Bacon 286, Product Code 22286. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA
    Category
    Food
    Distribution
    10 states
  • SevereFDA (Food)·F-0118-2017·2016-10-26

    Awareness Boost Tea Recalled for Potential Salmonella Contamination

    Awareness Corporation is recalling 2,697 bottles of Boost Tea dietary supplement due to potential Salmonella contamination. The product was distributed in 34 U.S. states and D.C.

    Product
    Awareness Boost Tea Dietary Supplement Passion Fruit Net Wt 7.4 oz. Distributed by & for all inquiries: Awareness Corporation P.O. Box 2289 Chandler, AZ 85244
    Category
    Food
    Distribution
    33 states
  • SevereFDA (Devices)·Z-0185-2017·2016-10-26

    Windstone Medical Packaging Recalls Extremity Tray Kits Due to Sterility Concerns

    Windstone Medical Packaging is recalling 816 Extremity Tray kits because the included Medtronic gloves may have splits or holes that compromise sterility.

    Product
    Extremity Tray, Kit number AMS1200(B and AMS1200(C convenience custom kits used for general surgery in hospital operating room
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0199-2017·2016-10-26

    QualiTech Red Bell Pepper Recalled for Potential E. coli O121 Contamination

    QualiTech is recalling 4,150 lbs of red bell peppers due to potential E. coli O121 contamination. The product was distributed in ten US states and Canada.

    Product
    FE Red Bell Pepper, Product Code 22708. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA
    Category
    Food
    Distribution
    10 states
  • SevereFDA (Food)·F-0195-2017·2016-10-26

    QualiTech Recalls Green Bell Peppers Due to Potential E. coli O121 Contamination

    QualiTech, Inc. is recalling 300 lbs of green bell peppers due to potential E. coli O121 contamination. The product was distributed to multiple US states and Canada.

    Product
    FE Green Bell Pepper 338, Product Code 22338. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA
    Category
    Food
    Distribution
    10 states
  • SevereFDA (Devices)·Z-0233-2017·2016-10-26

    Windstone Medical Packaging Recalls Major Laparotomy Packs Due to Sterility Concerns

    Windstone Medical Packaging is recalling 12 Major Laparotomy Packs because the included Medtronic gloves may contain splits or holes that compromise sterility.

    Product
    Major Laparotomy Pack - NS, kit number AMS4347 convenience custom kits used for general surgery in hospital operating room
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0203-2017·2016-10-26

    QualiTech Recalls Frozen Red Bell Peppers Due to E. coli O121 Risk

    QualiTech is recalling frozen red bell peppers due to a potential presence of E. coli O121 bacteria reported by a supplier.

    Product
    FE RedBell Pepper, Product Code 22760. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA
    Category
    Food
    Distribution
    10 states
  • SevereFDA (Food)·F-0198-2017·2016-10-26

    QualiTech Recalls Cheddar Cheese Due to Potential E. coli O121 Presence

    QualiTech is recalling FE Cheddar Cheese because a supplier reported the potential presence of E. coli O121 bacteria.

    Product
    FE Cheddar Cheese, Product Code 22518. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA
    Category
    Food
    Distribution
    10 states
  • SevereFDA (Devices)·Z-0263-2017·2016-10-26

    Windstone Medical Recalls Plastic Packs with Defective Gloves

    Windstone Medical Packaging is recalling 204 plastic packs used in general surgery because the included Medtronic gloves may contain splits or holes that compromise sterility.

    Product
    Plastic Pack , Kit number AMS1833(A convenience custom kits used for general surgery in hospital operating room
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0202-2017·2016-10-26

    QualiTech Recalls Green Bell Peppers Due to E. coli O121 Risk

    QualiTech, Inc. is recalling specific lots of green bell peppers due to a potential presence of E. coli O121 bacteria identified by a supplier.

    Product
    FE Green Bell Pepper, Product Code 22733. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA
    Category
    Food
    Distribution
    10 states
  • SevereFDA (Food)·F-0206-2017·2016-10-26

    QualiTech Recalls FE Bacon Due to Potential E. coli O121 Presence

    QualiTech, Inc. is recalling 500 lbs of FE Bacon because a supplier notified them of potential E. coli O121 bacteria in the material.

    Product
    FE Bacon, Product Code 24117. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA
    Category
    Food
    Distribution
    10 states
  • SevereFDA (Food)·F-0201-2017·2016-10-26

    QualiTech Recalls FE Rainbow Blend 714 Due to E. coli O121 Risk

    QualiTech is recalling FE Rainbow Blend 714 because a supplier notified them of potential E. coli O121 bacteria contamination.

    Product
    FE Rainbow Blend 714, Product Code 22714. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA
    Category
    Food
    Distribution
    10 states
  • SevereFDA (Food)·F-0196-2017·2016-10-26

    QualiTech Recalls Red Bell Peppers Due to Potential E. coli O121

    QualiTech is recalling 6,000 lbs of red bell peppers due to potential E. coli O121 contamination. The product was distributed to 10 US states and Canada.

    Product
    FE RedBell Pepper 339, Product Code 22339. 50 lb corrugated case with polyliner. Manufactured by: QualiTech, 318 Hazeltine Drive, Chaska, MN 55318 USA
    Category
    Food
    Distribution
    10 states
  • SevereFDA (Food)·F-0124-2017·2016-10-26

    Kabobs Recalls Mini Cheese Quiche Due to E. coli O121 Contamination

    Kabobs Inc is recalling 377 cases of Mini Cheese Quiche because the flour used was contaminated with E. coli O121. The product was distributed across 28 states.

    Product
    MINI CHEESE QUICHE, 200 CT, Prepared by: Kabobs, 54234 North Lake Dr. Lake City, GA 30260.
    Category
    Food
    Distribution
    27 states
  • SevereFDA (Devices)·Z-0253-2017·2016-10-26

    Windstone Medical Recalls Ortho Kits Due to Potential Sterility Compromise

    Windstone Medical Packaging is recalling 145 Ortho Kits because the disposable gloves included may contain splits or holes that compromise sterility.

    Product
    Ortho Kit, Kit number PSS1039(A and PSS1039(B convenience custom kits used for general surgery in hospital operating room
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0134-2017·2016-10-26

    Kabobs Four Cheese Puff Recalled Due to E. coli O121 Contamination

    Kabobs Inc is recalling Four Cheese Puff products because they were manufactured with flour contaminated with E. coli O121.

    Product
    FOUR CHEESE PUFF, 200 CT, Prepared by: Kabobs, 54234 North Lake Dr. Lake City, GA 30260
    Category
    Food
    Distribution
    27 states
  • HighFDA (Devices)·Z-0285-2017·2016-10-26

    Windstone Medical Recalls Dr. Fritsch Surgical Kits Due to Sterility Concerns

    Windstone Medical Packaging is recalling 224 Dr. Fritsch surgical kits because the included Medtronic gloves may have splits or holes that compromise sterility.

    Product
    Dr. Fritsch Pack, Kit number AMS2696 convenience custom kits used for general surgery in hospital operating room
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0147-2017·2016-10-26

    Windstone Medical Recalls Basic Surgery Kits Due to Sterility Compromise

    Windstone Medical Packaging is recalling 6,381 Basic Pack surgery kits because Medtronic gloves inside may have splits or holes that compromise sterility.

    Product
    Basic Pack, Kit part numbers AMS1388(A, AMS1520, AMS1868, AMS1868(A, AMS1868(B, AMS2608, AMS2608(A, AMS2728, AMS2728(A, AMS2758, AMS2758(A, AMS2972, AMS4264, AMS4309, PSS1833, and PSS1848(A. convenience custom kits used for general surgery in hospital operating room
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0296-2017·2016-10-26

    Ethicon Endo-Surgery Recalls Endoscopic Articulating Linear Cutters

    Ethicon Endo-Surgery Inc is recalling 213 Endoscopic Articulating Linear Cutters because a pinion gear failure could interrupt the firing stroke and expose healthcare professionals to sharps injuries.

    Product
    Endoscopic Articulating Linear Cutter, 38ATW35. VASCULAR/THIN 35MM The ENDOPATH ETS-Flex Endoscopic Articulating Linear Cutter has application in general, gynecologic, urologic, and thoracic surgery for transection, resection, and/or creation of anastomoses
    Category
    Medical Device
    Distribution
    37 states
  • HighFDA (Devices)·Z-0191-2017·2016-10-26

    Windstone Medical Recalls Foot Pack Kits Due to Sterility Concerns

    Windstone Medical Packaging is recalling 85 Foot Pack kits because the included Medtronic gloves may contain splits or holes that compromise sterility.

    Product
    Foot Pack, Kit number AMS3637 convenience custom kits used for general surgery in hospital operating room
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0190-2017·2016-10-26

    Medtronic Disposable Gloves Recalled for Potential Sterility Compromise

    Medtronic COVER LIGHT HANDLE DISPOSABLE GLOVES are being recalled because splits or holes may compromise sterility.

    Product
    Facial Tray, Kit number PSS1558(A convenience custom kits used for general surgery in hospital operating room
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0272-2017·2016-10-26

    Windstone Medical Packaging Recalls Student Pack-NS Surgical Kits

    Windstone Medical Packaging is recalling Student Pack-NS surgical kits because the Medtronic gloves included may have splits or holes that compromise sterility.

    Product
    Student Pack-NS, Kit number PSS2788 convenience custom kits used for general surgery in hospital operating room
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0194-2017·2016-10-26

    Windstone Medical Recalls General Surgery Kits Due to Sterility Concerns

    Windstone Medical Packaging is recalling 1,596 General Pack I surgery kits because the included Medtronic gloves may contain splits or holes that compromise sterility.

    Product
    General Pack I, Kit number CMP1811(B convenience custom kits used for general surgery in hospital operating room
    Category
    Medical Device
    Distribution
    Distributed nationwide