State

Minnesota product recalls

73,741 recalls have nationwide distribution and so reach Minnesota. 7,849 additional recalls listed Minnesota specifically in their distribution scope.

What the numbers show

Total: 7,849
Critical: 1,137
Severe: 2,245
Most recent: 2026-10-28

Of the 7,849 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 2,245 (29%) are Severe.

Which agencies issued them

These figures cover only the 7,849 recalls whose distribution notice names Minnesota specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

39501–39525 of 81590

HighFDA (Devices)·Z-0535-2019·2018-12-12
Zimmer Biomet Recalls Guide Wires Due to Sterility Compromise
Zimmer Biomet is recalling ZMS Intramedullary Fixation Smooth Guide Wires because creases in the sealing area may compromise product sterility.
Product
Zimmer ZMS¿ Intramedullary Fixation Smooth Guide Wire - Bullet Tip, 3.0 mm Diameter, 100 cm Length Item Number: 47-2237-038-00 Product Usage: A single use surgical instrument used during orthopaedic surgery for implantation of a prosthesis.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0530-2019·2018-12-12
Zimmer Biomet Recalls Pressure Sentinel Guide Wires Due to Sterility Compromise
Zimmer Biomet is recalling Pressure Sentinel Guide Wires because creases in the sealing area compromise product sterility. The recall affects 48,320 units distributed worldwide.
Product
Zimmer Pressure Sentinel¿ Intramedullary Reaming System, Guide Wire, Bullet Tip, 2.4 mm Diameter Item Number: 00-2228-024-00 Product Usage: A single use surgical instrument used during orthopaedic surgery for implantation of a prosthesis.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·18V886000·2018-12-12
Gillig Recalls 2016-2017 Low Floor Buses Due to Emergency Exit Defect
Gillig is recalling 2016-2017 Low Floor transit buses because an emergency exit window may be obstructed, hindering evacuation.
Product
GILLIG — GILLIG LOW FLOOR
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0537-2019·2018-12-12
Zimmer Biomet Recalls Smooth Guide Wires Due to Sterility Compromise
Zimmer Biomet is recalling Smooth Guide Wires because creases in the sealing area may compromise product sterility. The recall affects 48,320 units distributed worldwide.
Product
Zimmer Smooth Guide Wire - Bullet Tip, 3.0 mm Diameter, 100 cm Length Item Number: 47-2255-008-01 Product Usage: A single use surgical instrument used during orthopaedic surgery for implantation of a prosthesis.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0547-2019·2018-12-12
Philips Brilliance 10 Slice CT Scanner Recalled for Gantry Cover Failure Risk
Philips is recalling Brilliance 10 Slice CT scanners because fiberglass resin may separate, causing the gantry front cover and metal support to fail or fall.
Product
Brilliance 10 Slice (Air), Model 728251 Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional Images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. These devices may include signal…
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·19047·2018-12-12
White-Rodgers Recalls Emerson Sensi WiFi Thermostats Due to Fire Hazard
White-Rodgers is recalling Emerson branded Sensi WiFi thermostats because contact between wires and household voltage can cause fire. No injuries have been reported.
Product
Emerson Branded Sensi WiFi thermostats
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0540-2019·2018-12-12
Zimmer Biomet Recalls Natural Nail System Guide Wires Due to Sterility Concerns
Zimmer Biomet is recalling 12,724 units of Natural Nail System Tear Drop Guide Wires because creases in the packaging may compromise sterility.
Product
Zimmer Natural Nail¿ System - Tear Drop Guide Wire, 3.0 mm Diameter, 70 cm Length Item Number: 47-2490-098-00 Product Usage: A single use surgical instrument used during orthopaedic surgery for implantation of a prosthesis.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0548-2019·2018-12-12
Philips Brilliance 6 Slice CT Scanner Recalled for Gantry Cover Separation Risk
Philips Medical Systems is recalling Brilliance 6 Slice CT scanners because fiberglass resin may separate, causing the gantry front cover to fail or fall.
Product
Brilliance 6 Slice (Air), Model 728256 Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional Images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. These devices may include signal…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·18V882000·2018-12-12
Van Hool Recalls 2015-2018 Buses Due to Fire Extinguisher Defect
Van Hool is recalling 2015-2018 TD925 and TDX25 buses because the fire suppression system actuator may fail to discharge during a fire.
Product
VAN HOOL — VAN HOOL TD925, TDX25
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0557-2019·2018-12-12
Stephanix D2RS Digital Dynamic Remote System Recalled for Table Movement Risk
Stephanix is recalling 17 D2RS Digital Dynamic Remote Systems because the table may continue moving after a command is released.
Product
STEPHANIX D2RS Digital Dynamic Remote Systemhttp://cts.fda.gov/division-tracking/images/trash.png Product The D2RS Digital Dynamic Remote System is indicated for use in generating fluoroscopic images of human anatomy for vascular angiography, diagnostic and interventional…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0541-2019·2018-12-12
Zimmer Biomet Recalls Natural Nail System Tear Drop Guide Wires
Zimmer Biomet is recalling Natural Nail System Tear Drop Guide Wires due to creases in the sealing area that compromise sterility.
Product
Zimmer Natural Nail¿ System - Tear Drop Guide Wire, 2.4 mm Diameter, 70 cm Length Item Number: 47-2490-098-01 Product Usage: A single use surgical instrument used during orthopaedic surgery for implantation of a prosthesis.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0546-2019·2018-12-12
Philips Brilliance 16 Slice CT Scanner Recall for Cover Separation
Philips is recalling Brilliance 16 Slice CT scanners because fiberglass resin may separate, causing the gantry front cover to fail or fall.
Product
Brilliance 16 Slice (Air), Model 728246 Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional Images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. These devices may include signal…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0543-2019·2018-12-12
Philips Brilliance 64 CT Scanner Recall for Gantry Cover Separation Risk
Philips Medical Systems is recalling Brilliance 64 CT scanners due to a potential fiberglass resin separation that could cause the gantry front cover to fail and fall.
Product
Brilliance 64, Model 728231 Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional Images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. These devices may include signal analysts and…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0553-2019·2018-12-12
Zimmer Biomet Recalls 20mm Compress Device Short Anchor Plug
Zimmer Biomet is recalling 6 units of the 20mm Compress Device Short Anchor Plug due to potential metal burrs that may prevent proper insertion of drill and transverse pins.
Product
Biomet 20mm Compress Device Short Anchor Plug With Drill Set / With Pin Inserter Ion Implant Item number: 178562 Product Usage: 1. Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement. 2. Tumor resections. 3. Revision of previously…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0556-2019·2018-12-12
Pfizer Recalls Thermacare Heatwraps Due to Material Leakage
Pfizer is recalling specific lots of Thermacare Heatwraps because the wraps may come apart and leak granular material.
Product
Thermacare HEATWRAPS JOINT PAIN THERAPY, 8 HEATWRAPS; MUSCLE PAIN THERAPY, 3 HEATWRAPS a) UPC 0573301311 b) UPC 0573301311 Product Usage: Provides heat therapy for temporary relief of minor muscular and joint aches and pains associated with overexertion, sprains, and…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0555-2019·2018-12-12
Pfizer Recalls Thermacare HeatWraps Menstrual Due to Material Leakage
Pfizer is recalling Thermacare HeatWraps Menstrual because the wraps may come apart and leak granular material.
Product
Thermacare HeatWraps Menstrual a) UPC 0573302002 b) UPC 0573302044 Product Usage: Provides heat therapy for temporary relief of minor menstrual cramp pain and associated back aches.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0693-2019·2018-12-12
Tillamook Ice Cream Recalled for Undeclared Color Additives
Tillamook County Creamery is recalling Chocolaty Chip Cookie Dough ice cream because it contains undeclared color additives Amaranth and Yellow No. 6.
Product
Chocolaty Chip Cookie Dough ice cream (item #67016), packaged in 1.75 qt. container. UPC 0 72830 07016 4. The label is read in parts: "***Tillamook ***ICE CREAM *** CHOCOLATY CHIP COOKIE DOUGH *** CONTAINS: MILK, WHEAT, SOY, TREE NUTS (COCONUT), EGG. IT IS MADE WITH…
Category
Food
Distribution
11 states
ModerateFDA (Devices)·Z-0559-2019·2018-12-12
Tosoh AIA-360 Analyzer Recalled for Labeling Clarifications on Maintenance Requirements
Tosoh Bioscience is recalling 1,228 AIA-360 Analyzers to update labeling and training materials regarding maintenance and reagent requirements.
Product
AIA-360 Analyzer, product code 019945/019945R The Tosoh AIA-360 Automated Immunoassay Analyzer is for use in vitro diagnostic to provide testing for a broad menu of assays in a unique patented dry reagent format.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0528-2019·2018-12-12
Becton Dickinson Recalls Trypticase Soy Agar Plates Due to Growth Inhibition
Becton Dickinson is recalling 54,300 plates of Trypticase Soy Agar with 5% Sheep Blood because a manufacturing error inhibited the growth of Gram-negative organisms.
Product
BD BBL Trypticase Soy Agar with 5% Sheep Blood, Catalog No. 221261, (non-selective, non-differential)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0692-2019·2018-12-12
Tillamook Mudslide Ice Cream Recalled for Undeclared Color Additives
Tillamook Mudslide ice cream is recalled because it contains trace amounts of undeclared color additives Amaranth and Yellow No. 6.
Product
Tillamook Mudslide ice cream (item #63006), packaged in 3 gallon tub. UPC 0 72830 63006 1. The label is read in parts: "***TILLAMOOK MUDSLIDE ICE CREAM*** ALLERGEN INFORMATION: This product contains milk, peanut, soy, tree nut (coconut), egg. It is made with equipment that…
Category
Food
Distribution
11 states
ModerateFDA (Devices)·Z-0554-2019·2018-12-12
Pfizer Recalls Thermacare HeatWraps Due to Leaking Granular Material
Pfizer is recalling Thermacare Muscle Pain Therapy HeatWraps because the wraps may come apart and leak granular material.
Product
Thermacare Muscle Pain Therapy HeatWraps: a) UPC 0573301314 b) UPC 0573301303 Product Usage: Provides heat therapy for temporary relief of minor muscular and joint aches and pains associated with overexertion, sprains, and arthritis.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0694-2019·2018-12-12
Tillamook Vanilla Chocolate Chip Ice Cream Recalled for Undeclared Color Additives
Tillamook is recalling Vanilla Chocolate Chip ice cream because it contains undeclared color additives Amaranth and Yellow No. 6.
Product
Vanilla Chocolate Chip ice cream (item #67017), packaged in 1.75 qt. container. UPC 0 72830 07017 1. The label is read in parts: "***Tillamook*** ICE CREAM*** VANILLA CHOCOLATE CHIP *** CONTAINS: MILK, TREE NUTS (COCONUT), EGG. IT IS MADE WITH EQUIPMENT THAT ALSO MAKES…
Category
Food
Distribution
11 states
ModerateFDA (Food)·F-0695-2019·2018-12-12
Tillamook Udderly Chocolate Ice Cream Recalled for Undeclared Color Additives
Tillamook is recalling Udderly Chocolate ice cream because it contains trace amounts of undeclared color additives Amaranth and Yellow No. 6.
Product
Udderly Chocolate ice cream (item #67045), packaged in 1.75 qt. container. UPC 0 72830 07045 4. The label is read in parts: "***Tillamook*** ICE CREAM*** UDDERLY CHOCOLATE *** CONTAINS: MILK, TREE NUTS (COCONUT), SOY, EGG. IT IS MADE WITH EQUIPMENT THAT ALSO MAKES PRODUCTS…
Category
Food
Distribution
11 states
LowFDA (Devices)·Z-0529-2019·2018-12-12
Helena Laboratories Recalls Gel Alkaline Phosphatase Isoenzyme Control Kits
Helena Laboratories is recalling 43 Gel Alkaline Phosphatase Isoenzyme Control Kits due to customer complaints of lower enzyme activity.
Product
Gel Alkaline Phosphatase Isoenzyme Control Kit: Gel Alkaline Phosphatase Isoenzyme Control Cat. No. 5104 1 x 2.0 mL FOR IN-VITRO DIAGNOSTIC USE Gel Alkaline Phosphatase Isoenzyme Control 20mL 001831 Alkaline Phosphatase Isoenzyme Control is to be used as a…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0289-2019·2018-12-12
Aurobindo Recalls Amlodipine and Olmesartan Medoxomil Tablets Due to Discoloration
Aurobindo Pharma USA Inc. is recalling Amlodipine and Olmesartan Medoxomil tablets because they were found to be pink instead of the expected cream color.
Product
AMLODIPINE AND OLMESARTAN MEDOXOMIL — AMLODIPINE AND OLMESARTAN MEDOXOMIL (AMLODIPINE AND OLMESARTAN MEDOXOMIL)
Category
Drug
Distribution
Distributed nationwide