State

Minnesota product recalls

73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

42801–42825 of 81660

HighFDA (Devices)·Z-1665-2018·2018-05-16
Baxter Sigma Spectrum Infusion Pump Recalled for Documentation Errors
Baxter Healthcare is recalling 444 Sigma Spectrum Infusion Pumps because technicians incorrectly documented that all final release tests were completed, when several were actually omitted.
Product
Baxter Sigma Spectrum Infusion Pump with Master Drug Library (Version 6) 35700BAXR Product Usage: The Baxter Sigma Spectrum Infusion Pump with master Drug Library is intended to be used for the controlled administration of fluids. These fluids may includes pharmaceutical…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1394-2018·2018-05-16
NatureBox Recalls Whole Wheat Chocolate Animal Cookies Due to Undeclared Soy
NatureBox is recalling specific lots of Whole Wheat Chocolate Animal Cookies because they may contain undeclared soy lecithin.
Product
Whole Wheat Chocolate Animal Cookies; 5 oz. pouch, 5 lb. Corporate bags UPC: 8 58950 00508 6 Ingredients: Whole Wheat Flour, Unbleached Enriched Wheat Flour (niacin, reduced iron, thiamine mononitrate, riboflavin, folic acid). soluble Corn Prebiotic Fiber, Granulated sugar…
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1749-2018·2018-05-16
DePuy Mitek Recalls Latarjet EXPERIENCE Sharp Curved Ostetome
DePuy Mitek is recalling 84 units of the Latarjet EXPERIENCE Sharp Curved Ostetome due to reports of the product loosening or coming unscrewed from the handle.
Product
LATARJET EXPERIENCE Sharp Curved Ostetome Product Usage: The Latarjet EXPERIENCE Instability Shoulder Set is intended to provide to the orthopedic surgeon with a means of bone fixation and to assist in the management of reconstructive surgeries.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1758-2018·2018-05-16
Synthes Sciatic Nerve Retractor Recalled for Potential Microspore Formation
Synthes (USA) Products LLC is recalling 235 Sciatic Nerve Retractors due to a potential for microspores to form on the hollow handle, which could allow fluid entry.
Product
Retractor f/Sciatic Nerve; Part number: 03.100.013; UDI: 10886982070623
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1738-2018·2018-05-16
Zimmer Biomet Recalls Gentle Threads Interference Screws Due to Sterilization Issue
Zimmer Biomet is recalling 54 Gentle Threads interference screws because overexposure to ethylene oxide sterilization may compromise the sterile barrier, potentially leading to infection.
Product
Gentle Threads, Interference Screw; Model No. 905608, for soft tissue reattachment procedures in the ankle/foot and knee.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1736-2018·2018-05-16
Zimmer Biomet Recalls Gentle Threads Interference Screws Due to Sterilization Issues
Zimmer Biomet is recalling 53 Gentle Threads Interference Screws because overexposure to ethylene oxide sterilization may have compromised the sterile barrier, potentially leading to infection.
Product
Gentle Threads, Interference Screw; Model No. 905605, for soft tissue reattachment procedures in the ankle/foot and knee.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1683-2018·2018-05-16
Siemens Recalls IMMULITE Assays Due to Biotin Interference Risk
Siemens Healthcare Diagnostics is recalling specific IMMULITE assay lots because the instructions fail to list biotin interference concentrations, potentially causing inaccurate test results.
Product
IMMULITE 2000/IMMULITE ¿ 2000 XPi OM-MA (CA125)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1697-2018·2018-05-16
Straumann Emdogain Recalled for Unverified Raw Material Shelf Life Change
Straumann Manufacturing is recalling Emdogain multipacks because a raw material shelf-life change was implemented without submitting data to demonstrate continued product efficacy.
Product
Straumann¿ Emdogain 0.7 ml Multipack USA. Enamel Matrix Derivative. Article Number 075.115
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1633-2018·2018-05-16
Vygon Recalls PICC Insertion Kits Due to Sterility Risk
Vygon U.S.A. is recalling 16,520 PICC Kit units (Product Code AMS-7063-1) because potential friction holes may compromise product sterility.
Product
PICC Kit, Product Code: AMS-7063-1 Convenience kit for the insertion of PICCs into the vascular system.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1670-2018·2018-05-16
Siemens Dimension Sirolimus Reagent Cartridge Recalled for Biotin Interference
Siemens Healthcare Diagnostics is recalling Dimension Sirolimus reagent cartridges because biotin can interfere with test results, potentially affecting patient care.
Product
Dimension¿ Sirolimus (SIRO) Flex¿ reagent cartridge
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1669-2018·2018-05-16
Siemens Dimension Free Thyroxine Reagent Cartridge Recall for Labeling Error
Siemens is recalling Dimension Free Thyroxine reagent cartridges because the instructions for use incorrectly state the level at which biotin does not interfere.
Product
Dimension¿ Free Thyroxine (FT4L) Flex¿ reagent cartridge
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1668-2018·2018-05-16
Siemens Recalls Dimension TSHL Reagent Cartridges Due to Biotin Labeling Error
Siemens Healthcare Diagnostics is recalling Dimension TSHL reagent cartridges because the instructions for use incorrectly state the biotin concentration level at which interference does not occur.
Product
Dimension¿ Thyroid Stimulating Hormone (TSHL) Flex¿ reagent cartridge
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1765-2018·2018-05-16
Bard POWERPORT ClearVUE Slim Catheter Recalled for Incorrect Patient ID Card Instructions
Bard Peripheral Vascular Inc is recalling 383 units of POWERPORT ClearVUE Slim catheters because the packaged Patient ID Card contains incorrect port flushing instructions.
Product
POWERPORT ClearVUE Slim with Smooth Septum, 8F ChronoFlex, Polyurethane Catheter with Open Suture Holes, REF 1678301
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1801-2018·2018-05-16
Beaver-Visitec Recalls Hemostatic Eraser Bipolar Due to Incorrect Labeling
Beaver-Visitec International Inc. is recalling 1,025 units of Wet-Field Hemostatic Eraser Bipolar 25G instruments because they were packaged with incorrect labeling.
Product
Wet-Field Hemostatic Eraser Bipolar 25G, fine tip, straight, 5/SP; Part Number 221267; UDI: 30886158010549
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1402-2018·2018-05-16
Peaceful Mountain Nasal Rescue Recalled as Unapproved New Drug
Grato Holdings is recalling Peaceful Mountain Nasal Rescue dietary supplements because they are unapproved new drugs based on disease claims.
Product
Peaceful Mountain, Nasal Rescue, Dietary Supplement, Natural Sinus Support, Dist. by Peaceful Mountain, Inc. Woodbine, IA 51579
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1759-2018·2018-05-16
Synthes Sciatic Nerve Retractor Recalled for Potential Microspore Formation
Synthes (USA) Products LLC is recalling 196 Sciatic Nerve Retractors due to a potential for microspores to form on the hollow handle, which could allow fluid entry.
Product
Retractor f/Sciatic Nerve Long; Part number: 03.100.014; UDI: 10886982070630
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1772-2018·2018-05-16
Bard POWERPORT ClearVUE Implantable Port Recall for Incorrect Instructions
Bard Peripheral Vascular Inc is recalling 15 units of POWERPORT ClearVUE isp Implantable Port kits because the included Patient ID Card contains incorrect port flushing instructions.
Product
POWERPORT ClearVUE isp Implantable Port With Smooth Septum and Attachable 8F Polyurethane Open-Ended Single-Lumen Venous Catheter Custom Kit, REF CP00004
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1689-2018·2018-05-16
Siemens ADVIA Centaur Folate Recalled for Biotin Interference Risk
Siemens Healthcare Diagnostics is recalling ADVIA Centaur Folate assays because biotin interference levels are not listed in the instructions, potentially affecting test accuracy.
Product
ADVIA Centaur¿ Folate (FOL)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1778-2018·2018-05-16
Siemens Syngo.Via Software Recall for Report Functionality Defect
Siemens Medical Solutions is recalling Syngo.Via VB20A software because corrected report values are not saved or transmitted, causing the system to use original values.
Product
Syngo.Via VB20A model 1049610
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1768-2018·2018-05-16
Bard POWERPORT ClearVUE Slim Catheter Recalled for Incorrect Flushing Instructions
Bard Peripheral Vascular Inc is recalling 3,196 units of POWERPORT ClearVUE Slim catheters because the included Patient ID Card contains incorrect port flushing instructions.
Product
POWERPORT ClearVUE Slim with Smooth Septum, 6F ChronoFlex Silk, Polyurethane Catheter, REF 5676300
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1764-2018·2018-05-16
Bard POWERPORT ClearVUE Slim Catheter Recalled for Incorrect Patient Card Instructions
Bard Peripheral Vascular Inc is recalling POWERPORT ClearVUE Slim catheters because the included Patient ID Card contains incorrect port flushing instructions.
Product
POWERPORT ClearVUE Slim with Smooth Septum, 8F ChronoFlex, Polyurethane Catheter, REF 1678300
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-1403-2018·2018-05-16
Energique Enervimin CNCR Focus Recalled as Unapproved New Drug
Grato Holdings, Inc. is recalling Energique Enervimin CNCR Focus dietary supplements because they are unapproved new drugs based on disease claims.
Product
Energique, Dietary Supplement, Enervimin CNCR Focus, Dist. by Energique Inc.. Woodbine, IA 51579
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1676-2018·2018-05-16
Siemens IMMULITE 2000 Folic Acid Assay Recalled for Biotin Interference
Siemens Healthcare Diagnostics is recalling IMMULITE 2000 Folic Acid assays because biotin interference is not listed in the instructions for use.
Product
IMMULITE ¿ 2000/IMMULITE ¿ 2000 XPi Folic Acid
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1678-2018·2018-05-16
Siemens IMMULITE CEA Assay Recalled for Biotin Interference Risk
Siemens Healthcare Diagnostics is recalling IMMULITE CEA assays because biotin interference thresholds are not listed in the instructions, potentially affecting test accuracy.
Product
IMMULITE ¿ /IMMULITE ¿ 1000 CEA
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1693-2018·2018-05-16
Straumann Emdogain Recalled Due to Unverified Raw Material Shelf Life Changes
Straumann Manufacturing is recalling Emdogain Enamel Matrix Derivative because a raw material shelf life change was implemented without submitting data to demonstrate continued product efficacy.
Product
Straumann¿ Emdogain 0.15 ml 5-Pack. Enamel Matrix Derivative. Article Number 075.098W
Category
Medical Device
Distribution
Distributed nationwide