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.

47801–47825 of 81668

  • SevereFDA (Drugs)·D-0872-2017·2017-06-07

    SCA Pharmaceuticals Recalls Fentanyl Injection Bags Due to Seam Leaks

    SCA Pharmaceuticals is recalling 118 bags of fentanyl injection due to seam leaks that compromise sterility. The product was distributed nationwide in the USA.

    Product
    fentaNYL (as citrate) in 0.9% Sodium Chloride injectable,10 mcg per mL, Total Volume 100 mL, Single Dose Container bag, (Total fentanyl Dose 1,000 mcg/100 mL) Preservative Free, Rx Only, SCA Pharmaceuticals, 8821 Knoedl Ct. Little Rock, AR 72205, NDC 70004-0229-32
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0873-2017·2017-06-07

    SCA Pharmaceuticals Recalls Fentanyl Injection Bags Due to Sterility Concerns

    SCA Pharmaceuticals is recalling 370 bags of fentanyl injection solution because the bags were leaking at the seam, compromising sterility.

    Product
    fentaNYL (as citrate) in 0.9% Sodium Chloride injectable,10 mcg per mL, Total Volume 100 mL, Single Dose Container bag, (Total fentanyl Dose 1,000 mcg/100 mL) Preservative Free, Rx Only, SCA Pharmaceuticals, 8821 Knoedl Ct. Little Rock, AR 72205, NDC 70004-0202-32
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2283-2017·2017-06-07

    Trident Battered Cod Recalled Due to Potential Plastic Contamination

    Trident Seafoods is recalling frozen Battered Cod Diamonds because they may contain small pieces of plastic.

    Product
    Trident Item # 474568, Irregulars Battered Cod 3 oz Battered Diamonds, food service packages, frozen, Net wt. 10 lbs.
    Category
    Food
    Distribution
    26 states
  • HighFDA (Devices)·Z-2175-2017·2017-06-07

    Philips NMT Patient Cable Recall for Potential Skin Burn Risk

    Philips is recalling NMT Patient Cables used with IntelliVue NMT Modules because a manufacturing defect may cause localized heating and skin burns.

    Product
    NMT Patient Cable (989803174581) in use with lntelliVue NMT Module (Part# 865383)
    Category
    Medical Device
    Distribution
    31 states
  • HighFDA (Devices)·Z-2179-2017·2017-06-07

    GE Healthcare Recalls Patient Steps on RFX, Legacy, and Precision 500D Systems

    GE Healthcare is recalling 2,380 patient steps for RFX, Legacy, and Precision 500D systems because they may detach from the table, posing a fall risk.

    Product
    Table Patient Step on RFX/SFX, Legacy, and Precision 500D systems
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2247-2017·2017-06-07

    Tyson Recalls Frozen Spinach Quiche Due to Listeria Risk

    Tyson Foods is voluntarily recalling specific lots of frozen Chef Pierre and Sara Lee spinach quiche due to a Listeria monocytogenes contamination risk from an ingredient supplier.

    Product
    Chef Pierre 10 Spinach Quiche, and 6/10 Frozen Quiche, 38 oz. packed in a paper carton, keep frozen
    Category
    Food
    Distribution
    14 states
  • HighFDA (Devices)·Z-2176-2017·2017-06-07

    AbbVie Recalls 673 PEG Kits Due to Sterility Concerns

    AbbVie Inc. is voluntarily recalling 673 PEG kits because they may not be sterile. The recall covers lots distributed nationwide and internationally.

    Product
    AbbVie PEG, PEG Kit 20FR, FOR ENTERAL USE ONLY, STERILE, Rx Only.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2217-2017·2017-06-07

    Cardinal Digital Bariatric Scales Recalled Due to Seat Failure Risk

    Cardinal Scale Mfg Co is recalling 975 digital bariatric scales because a seat may fail unexpectedly, posing an injury risk.

    Product
    Cardinal, Digital Bariatric Scale 1) model 6876, Cap 600 and 2) model 6868 Cap 1000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-2277-2017·2017-06-07

    Trident Multi-Grain Alaskan Cod Recalled for Plastic Contamination

    Trident Seafoods is recalling 12 oz. packages of Multi-Grain Alaskan Cod because they may contain small pieces of plastic.

    Product
    Trident Item # 421048, Multi-Grain Alaskan Cod, Frozen, RETAIL packages, Net wt. 12 oz. UPC 0 28029 21048 4 The retail label is read in parts: "***Trident SEAFOODS***Multi-Grain Alaskan Cod***NET WT. 12 OZ.***". The retail case label is read in parts: "***Trident…
    Category
    Food
    Distribution
    26 states
  • HighFDA (Food)·F-2279-2017·2017-06-07

    Trident Alaska Cod Squares Recalled for Potential Plastic Contamination

    Trident Seafoods is recalling frozen Alaska Cod Squares because they may contain small pieces of plastic.

    Product
    Trident Item # 16595, Alaska Cod Squares 4 oz, raw breaded panko, food service packages, frozen, Net wt. 10 lbs.
    Category
    Food
    Distribution
    26 states
  • HighFDA (Food)·F-2248-2017·2017-06-07

    Tyson Recalls Frozen Quiche Products Due to Listeria Risk

    Tyson Foods is voluntarily recalling specific lots of frozen quiche products because an ingredient supplier recalled items due to Listeria monocytogenes.

    Product
    Sara Lee CP Quiche 10 Spinach , 38 oz. packed in a paper carton, keep frozen
    Category
    Food
    Distribution
    14 states
  • HighFDA (Devices)·Z-2198-2017·2017-06-07

    Zimmer Biomet Recalls Reusable Orthopedic Instruments Due to Durability Concerns

    Zimmer Biomet is recalling reusable instruments for knee, hip, trauma, and extremities because their durability characteristics were not established.

    Product
    Reusable instruments in the Knee, Hip, Trauma, and Extremities segments.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2171-2017·2017-06-07

    KCI USA Recalls 1000 ml Canisters for Negative Pressure Wound Therapy Systems

    KCI USA is recalling 5,385 cases of 1000 ml canisters for InfoV.A.C. and V.A.C.ULTA systems due to a potential sterile barrier breach.

    Product
    1000 ml Canister (with Gel) for InfoV.A.C. and V.A.C.ULTA Therapy Systems (Part Number M8275093/5). The InfoV.A.C. and V.A.C.ULTA Negative Pressure Wound Therapy Systems are integrated wound management systems for use in acute, and extended and care settings. They are…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2152-2017·2017-06-07

    Hans Pausch Uroview FD Fluoroscopic X-ray System Recalled for Footswitch Safety Issue

    Hans Pausch is recalling 10 Uroview FD fluoroscopic X-ray systems because the footswitch used to activate radiation is part of the safety circuit.

    Product
    Pausch Uroview FD fluoroscopic X-ray system UDI number (01)04260491620040 Primarily for urological applications (functional X-ray diagnostics, endourology and minimal invasive urology / surgery). The system, which includes a radiologic / urologic treatment table, maybe used…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2215-2017·2017-06-07

    Zimmer Biomet Recalls AFFIXUS Hip Fracture Nail Due to Sizing Defect

    Zimmer Biomet is recalling 33,500 AFFIXUS Hip Fracture Nail units worldwide because certain undersized specifications may prevent the nail from properly engaging with the targeting jig.

    Product
    AFFIXUS Hip Fracture Nail Product Usage: The Hip Fracture Nail System is intended to treat stable and unstable proximal fractures of the femur including pertrochanteric fractures, interochanteric fractures, high subtrochanteric fractures and combinations of these fractures…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2280-2017·2017-06-07

    Trident Alaska Cod Diamond Cut Squares Recalled for Plastic Contamination

    Trident Seafoods is recalling frozen Alaska Cod Diamond Cut Squares because they may contain small pieces of plastic.

    Product
    Trident Item # 16596, Alaska Cod Diamond Cut 3 oz, English Style Battered Deep Fry, food service packages, frozen, Net wt. 10 lbs.
    Category
    Food
    Distribution
    26 states
  • ModerateFDA (Devices)·Z-2173-2017·2017-06-07

    Roche Recalls PreciControl Varia 3 Due to Typographical Error

    Roche Diagnostics is recalling 1,603 units of Elecsys PreciControl Varia 3 because the e-barcode and value sheet contain a typographical error for PTH target values.

    Product
    Elecsys PreciControl Varia 3
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2177-2017·2017-06-07

    AbbVie Recalls PEG Kits Due to Missing or Duplicate Components

    AbbVie is recalling specific lots of PEG Kits due to potential defects including missing components, duplicate parts, or missing labels and instructions.

    Product
    AbbVie PEG, PEG Kit 15FR, FOR ENTERAL USE ONLY, STERILE, Rx Only.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2278-2017·2017-06-07

    Trident Panko Breaded Alaska Cod Recalled for Plastic Contamination

    Trident Seafoods is recalling Panko Breaded Alaska Cod because it may contain small pieces of plastic.

    Product
    Trident Item # 38520, Panko Breaded Alaska Cod, 4 oz. Square Portions Raw, Food Service packages, frozen, Net Wt. 10 lbs.
    Category
    Food
    Distribution
    26 states
  • ModerateFDA (Devices)·Z-2109-2017·2017-06-07

    Toshiba Angio WorkStation Recalled for Dose Tracking Display Error

    Toshiba is recalling 70 Angio WorkStation units because the Peak Skin Dose value may display incorrectly if the workstation is powered on after the Infinix system.

    Product
    Angio WorkStation (XIDF-AWS801) used in conjunction with your Infinix System (INFX-8000V;INFX-8000C;INFX-8000F
    Category
    Medical Device
    Distribution
    28 states
  • ModerateFDA (Devices)·Z-2166-2017·2017-06-07

    Siemens SHBG Immulite 2000 Reagent Recall Due to Stability Issues

    Siemens is recalling certain lots of SHBG Immulite 2000 reagents because they may not meet stability claims, potentially causing test bias.

    Product
    SHBG IMMULITE 2000/IMMULITE 2000 XPi For the in vitro diagnostic use with the IMMULITE 2000 Systems Analyzers-For the quantitative measurement of SHBG in serum, as aid in the differential diagnosis of hirsutism.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2282-2017·2017-06-07

    Trident Alaska Cod Rectangles Recalled for Potential Plastic Contamination

    Trident Seafoods is recalling frozen Alaska Cod Rectangles because they may contain small pieces of plastic.

    Product
    Trident Item # 17116, Alaska Cod Rectangles 3 oz,Crunchy Breaded, food service packages, frozen, Net wt. 10 lbs.
    Category
    Food
    Distribution
    26 states