State

Minnesota product recalls

73,576 recalls have nationwide distribution and so reach Minnesota. 7,844 additional recalls listed Minnesota specifically in their distribution scope.

What the numbers show

Total: 7,844
Critical: 1,139
Severe: 2,243
Most recent: 2026-10-24

Of the 7,844 recalls naming Minnesota we have scored against our rubric, 1,139 (15%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,243 (29%) are Severe.

Which agencies issued them

These figures cover only the 7,844 recalls whose distribution notice names Minnesota specifically. The 73,576 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

25326–25350 of 81420

SevereFDA (Drugs)·D-0061-2022·2021-11-03
Methylcobalamin Injection Recalled for Sterility Assurance Deficiency
Red Mountain Compounding Pharmacy is recalling Methylcobalamin 5000 mcg/mL multi-dose vial injection due to lack of assurance of sterility identified during FDA inspection. The product was distributed to approximately 494 patients in Arizona, California, Florida, Minnesota, Montana, Texas, and Utah.
Product
METHYLCOBALAMIN 5000MCG/ML MDV INJ, Rx only, Red Mountain Compounding Rx
Category
Drug
Distribution
7 states
SevereFDA (Food)·F-0071-2022·2021-11-03
Nature's Heart Superfood Trail Mix recalled for undeclared peanuts
Nestle USA is recalling Nature's Heart Superfood Trail Mix 1.5oz pouches because they contain undeclared peanuts, posing a serious risk to consumers with peanut allergies.
Product
Nature's Heart Superfood Trail Mix 1.5oz poly film pouches - 32 units per case
Category
Food
Distribution
32 states
SevereFDA (Drugs)·D-0032-2022·2021-11-03
Ascorbic Acid Injectable Solution Recalled for Sterility Assurance Concerns
Red Mountain Compounding Pharmacy is recalling Ascorbic Acid (Non-Corn) 500mg/mL Solution for Injection due to lack of assured sterility identified during an FDA inspection. The affected product was distributed to approximately 494 patients in seven states.
Product
ASCORBIC ACID (NON-CORN) 500MG/ML SOLN (PF), Rx only, Red Mountain Compounding Rx
Category
Drug
Distribution
7 states
SevereFDA (Drugs)·D-0040-2022·2021-11-03
Levocarnitine Injectable Solution Recalled for Sterility Assurance Concerns
Red Mountain Compounding Pharmacy is recalling levocarnitine 100 mg/mL injectable solution (all lots within expiry) due to FDA inspection findings that raised sterility assurance concerns. Approximately 494 patients in seven states received prescriptions.
Product
LEVOCARNITINE 100MG/ML MDV SOLN, Rx only, Red Mountain Compounding Rx
Category
Drug
Distribution
7 states
SevereFDA (Drugs)·D-0063-2022·2021-11-03
MIC/B12A Injectable Compounded Drug Recall for Sterility Assurance
Red Mountain Compounding Pharmacy is recalling MIC/B12A 25/50/50MG/ML 1MG/ML MDV injectable medication because FDA inspection found the firm could not guarantee the sterility of the product. Approximately 494 patients across seven states received prescriptions for this medication.
Product
MIC/B12A 25/50/50MG/ML 1MG/ML MDV, Red Mountain Compounding Rx
Category
Drug
Distribution
7 states
SevereFDA (Drugs)·D-0047-2022·2021-11-03
TEST CYP/PROP Compounded Injection Recalled for Sterility Assurance Concerns
Red Mountain Compounding Pharmacy is recalling TEST CYP/PROP 160/40MG/ML MDV in ethyl oleate due to FDA inspection findings that raised concerns about sterility assurance. Approximately 494 patients in multiple states received affected prescriptions.
Product
TEST CYP/PROP 160/40MG/ML MDV IN ETHYL OLEATE, Rx only, Red Mountain Compounding Rx
Category
Drug
Distribution
7 states
SevereFDA (Food)·F-0073-2022·2021-11-03
Nature's Heart Pineapple Chili Cashew Mix Recalled for Undeclared Peanuts
Nestle USA is recalling Nature's Heart Pineapple Chili Cashew Glazed Mix due to undeclared peanut allergen. The product was distributed across 32 states, and consumers with peanut allergies should not consume it.
Product
Nature's Heart Pineapple Chili Cashew Glazed Mix 1.5oz poly film pouches - 32 units per case
Category
Food
Distribution
32 states
SevereFDA (Drugs)·D-0059-2022·2021-11-03
Methylcobalamin Injectable: Sterility Assurance Deficiency
Red Mountain Compounding Pharmacy is recalling methylcobalamin 1000 mcg/mL injectable due to FDA inspection findings that raised concerns about the product's sterility assurance.
Product
METHYLCOBALAMIN 1000MCG/ML MDV INJ, Rx only, Red Mountain Compounding Rx
Category
Drug
Distribution
7 states
SevereFDA (Drugs)·D-0031-2022·2021-11-03
Ascorbic Acid Solution Recalled Due to Sterility Assurance Concerns
Red Mountain Compounding Pharmacy is recalling Ascorbic Acid (Non-Corn) 500mg/mL multi-dose solution due to FDA inspection findings regarding lack of sterility assurance. The affected product was distributed to approximately 494 patients across seven states.
Product
ASCORBIC ACID (NON-CORN) 500MG/ML MDV SOLN, Rx only, Red Mountain Compounding Rx
Category
Drug
Distribution
7 states
SevereNHTSA·21V854000·2021-11-03
Mercedes-Benz Recalls One 2020 Sprinter for Incorrect Brake Discs
Daimler Vans USA is recalling one 2020 Mercedes-Benz Sprinter because incorrect-size front brake discs may extend stopping distance and increase crash risk.
Product
MERCEDES-BENZ — MERCEDES-BENZ SPRINTER (VS30)
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0058-2022·2021-11-03
Methylcobalamin Injectable Recalled Due to Sterility Assurance Concerns
Red Mountain Compounding Pharmacy is recalling methylcobalamin 10,000 MCG/ML multi-dose vials after FDA inspection identified sterility assurance concerns.
Product
METHYLCOBALAMIN 10,000MCG/ML MDV INJ, Rx only, Red Mountain Compounding Rx
Category
Drug
Distribution
7 states
HighFDA (Drugs)·D-0045-2022·2021-11-03
TEST CYP 25MG/ML Injectable Lacks Assurance of Sterility
Red Mountain Compounding Pharmacy is recalling TEST CYP 25MG/ML in Ethyl Oleate because FDA inspection raised concerns about sterility assurance. Approximately 494 patients in seven states received prescriptions for this drug.
Product
TEST CYP 25MG/ML IN ETHYL OLEATE MDV, Rx only, Red Mountain Compounding Rx
Category
Drug
Distribution
7 states
HighFDA (Devices)·Z-0165-2022·2021-11-03
GORE Cardioform Septal Occluder recalled for incorrect expiration date labeling
W.L. Gore is recalling 138 units of GORE Cardioform Septal Occluder devices labeled with a 3-year expiration date instead of the actual 2-year shelf life.
Product
REF/Catalogue Number GSX0020A, GORE CARDIOFORM SEPTAL OCCLUDER 20 mm Diameter, Catheter Working Length 75 cm, Delivery Profile 10 Fr, STERILE EO, Rx Only, UDI: 00733132631018
Category
Medical Device
Distribution
47 states
HighFDA (Drugs)·D-0054-2022·2021-11-03
Acetylcysteine 2% Ophthalmic Solution Recalled for Sterility Concerns
Red Mountain Compounding Pharmacy is recalling Acetylcysteine 2% Ophthalmic Solution due to lack of assurance of sterility. The FDA identified concerns during an inspection of the manufacturing facility.
Product
ACETYLCYSTEINE 2% OPTH SOLN, Rx only, Red Mountain Compounding Rx
Category
Drug
Distribution
7 states
HighFDA (Drugs)·D-0051-2022·2021-11-03
Vitamin B Complex Injectable Solution Recalled for Sterility Concerns
Red Mountain Compounding Pharmacy is recalling Vitamin B Complex Injectable Solution (HP) due to lack of assurance of sterility raised during FDA inspection. Approximately 494 patients across seven states received affected prescriptions.
Product
VIT B COMPLEX INJ SOLN (HP), Rx only, Red Mountain Compounding Rx
Category
Drug
Distribution
7 states
HighFDA (Drugs)·D-0062-2022·2021-11-03
MIC Compounded Injection Recalled Due to Sterility Assurance Concerns
Red Mountain Compounding Pharmacy is recalling MIC 25/50/50MG/ML MDV injectable medication due to lack of assurance of sterility following an FDA inspection. Approximately 494 patients in seven states received prescriptions for the affected product.
Product
MIC 25/50/50MG/ML MDV, Rx only,Red Mountain Compounding Rx
Category
Drug
Distribution
7 states
HighFDA (Devices)·Z-0181-2022·2021-11-03
Siemens Advia Chemistry Urinary Protein Reagent Recall for Inaccurate Test Results
Siemens is recalling Advia Chemistry Urinary/Cerebrospinal Fluid Protein reagent due to potential reagent carryover that may cause falsely depressed Hemoglobin A1c results, which could affect clinical decisions about patient treatment.
Product
Advia Chemistry Urinary/Cerebrospinal Fluid Protein (UCFP), SMN 11319151
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0055-2022·2021-11-03
Benzalkonium Chloride Solution Recalled Due to Sterility Concerns
Red Mountain Compounding Pharmacy is recalling Benzalkonium Chloride 0.013% Solution due to lack of assurance of sterility identified during an FDA inspection. Approximately 494 patients in seven states received prescriptions for this product.
Product
BENZALKONIUM CHLORIDE 0.013% SOLUTION, Rx only, Red Mountain Compounding Rx
Category
Drug
Distribution
7 states
HighNHTSA·21V853000·2021-11-03
Loose Brake Pipe Nut in 2022 Volkswagen Tiguan Vehicles
Volkswagen is recalling 2022 Tiguan vehicles with a loose brake pipe nut near the right-front wheel well. The loose nut could cause brake fluid to leak, reducing braking power and increasing crash risk.
Product
VOLKSWAGEN — VOLKSWAGEN TIGUAN
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0180-2022·2021-11-03
Siemens Atellica CH Protein Reagent Recalled for Carryover Affecting Test Results
Siemens Healthcare is recalling Atellica CH Urinary/Cerebrospinal Fluid Protein reagent due to potential carryover causing falsely depressed Hemoglobin A1c results that may affect clinical decision-making.
Product
Atellica CH Urinary/Cerebrospinal Fluid Protein (UCFP), SMN 11097543
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·21V852000·2021-11-03
2021 Volkswagen ID.4 Steering Gear Defect Poses Loss of Control Risk
Volkswagen is recalling one 2021 ID.4 vehicle with a defective steering gear. A missing or incorrectly assembled drive bushing may cause loss of steering control and increase crash risk.
Product
VOLKSWAGEN — VOLKSWAGEN ID.4
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0169-2022·2021-11-03
GORE CARDIOFORM Septal Occluder devices labeled with incorrect expiration date
W L Gore recalled 846 GORE CARDIOFORM Septal Occluder units labeled with a 3-year expiration instead of the correct 2-year expiration.
Product
REF/Catalogue Number GSXE0030, GORE CARDIOFORM SEPTAL OCCLUDER 30 mm Diameter, Catheter Working Length 75 cm, Delivery Profile 10 Fr, STERILE EO, Rx Only, UDI: 00733132617661 *Not distributed within the US
Category
Medical Device
Distribution
47 states
HighFDA (Devices)·Z-0176-2022·2021-11-03
ASC PneumoLiner surgical device recalled due to manufacturing orientation defect
Olympus recalls ASC PneumoLiner surgical devices due to incorrect orientation of the containment bag that deploys upside down. This increases the risk of trapping bowel tissue during gynecologic laparoscopic surgery.
Product
ASC PneumoLiner device, Part No. WA90500US (US market only) The Pneumoliner device is intended for use as a multiple instrument port and tissue containment system during minimally invasive gynecologic laparoscopic surgery to enable the isolation and containment of tissue…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0036-2022·2021-11-03
Dexpanthenol Injection Solution Recalled for Sterility Assurance Concerns
Red Mountain Compounding Pharmacy is recalling Dexpanthenol 250mg/mL injection solution due to FDA findings that sterility assurance cannot be confirmed. The product was distributed to approximately 494 patients across seven states.
Product
DEXPANTHENOL 250MG/ML INJ SOLN, Rx only, Red Mountain Compounding Rx
Category
Drug
Distribution
7 states
HighNHTSA·21V855000·2021-11-03
Rolls-Royce Recalls Phantom Vehicles Due to Rearview Camera Display Issue
Rolls-Royce is recalling 2019-2022 Phantom vehicles because the central display may not raise correctly, partially blocking the rearview camera image.
Product
ROLLS-ROYCE — ROLLS-ROYCE PHANTOM
Category
Vehicle
Distribution
Distributed nationwide