State

Minnesota product recalls

73,509 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 73,509 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

23401–23425 of 81353

HighFDA (Food)·F-0860-2022·2022-03-23
Herbalife Protein Bar Deluxe recalled for undeclared egg allergen
Herbalife International is recalling Herbalife NutritionProtein Bar Deluxe in Chocolate Peanut flavor nationwide due to undeclared egg allergen. The product poses a risk to consumers with egg allergies.
Product
Herbalife NutritionProtein Bar Deluxe - Chocolate Peanut flavor. 14 bars per carton Protein-based snack for energy and nutrition 14 bars 1.23 oz (35 g) each Net wt. 17.3 oz., (490 g) SKU: 0365US Catalog Number: 0365 Formulated and Distributed by Herbalife International of…
Category
Food
Distribution
Distributed nationwide
HighFDA (Food)·F-0871-2022·2022-03-23
Honey Sriracha Seasoning Recalled for Undeclared Wheat Allergen
PS Seasoning & Spices is recalling its Honey Sriracha Snack Stick Seasoning due to undeclared wheat. The product was distributed to multiple U.S. states and Canada.
Product
796-B Honey Sriracha Snack Stick Seasoning Net Wt 5.25 lbs. (2.38kg). Part #020001965. Ingredients: Sugar, Salt, Spice, Brown Sugar, Dried Honey, Hot Sauce Powder (aged Cayenne Red Peppers, Vinegar, Salt, Garlic), Garlic Powder, Sodium Diacetate, Sodium Erythorbate…
Category
Food
Distribution
27 states
HighFDA (Devices)·Z-0806-2022·2022-03-23
Syphilis Test Reagent Pack Recalled for Vaccine Interference and Manufacturing Defects
Bio-Rad's BioPlex 2200 Syphilis Test Reagent Pack is being recalled due to concerns that COVID-19 vaccines may interfere with test results, and due to manufacturing defects affecting reagent stability.
Product
BioPlex 2200 REF 12000650 SYPH T PACK Syphilis Total & RPR Reagent Pack
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0800-2022·2022-03-23
SAFE-T PLUS Adult Lumbar Puncture Tray recalled for manometer failure
Bard Peripheral Vascular Inc recalled 3,240 SAFE-T PLUS Adult lumbar puncture trays due to manometer failures involving leaking and defective mating connections.
Product
SAFE-T PLUS ATRAUMATIC ADULT LP TRAY
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0797-2022·2022-03-23
Lumbar Puncture Tray Devices Recalled for Manometer Leaking and Mating Issues
Bard Peripheral Vascular Inc. recalls SAFE-T PLUS lumbar puncture trays due to manometer leaking and mating issues affecting device function. The FDA Class II recall covers 15,650 devices distributed nationwide and internationally.
Product
SAFE-T PLUS LUMBARPUNCTURE TRAY ADULT
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0750-2022·2022-03-23
Hologic Panther Fusion Extraction Reagent-X May Produce False Test Results
Hologic is recalling Panther Fusion Extraction Reagent-X kits due to failed stability specifications that may cause false negative test results. Healthcare providers should stop using affected lots.
Product
Panther Fusion Extraction Reagent-X, REF PRD-04477, For use with Panther Fusion System, IVD, Rx only, Contents: FCR-X Fusion Capture reagent-X 4 EA, FER-X Fusion Enhancer Reagent-X (Lithium Hydroxide Solution) 4 EA
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0769-2022·2022-03-23
JAGTOME RX medical device recalled for sterile barrier breach
Boston Scientific's JAGTOME RX medical device (367 units) is being recalled worldwide due to a sterile barrier breach that compromises device sterility.
Product
JAGTOME RX 39-20-450-025 Material Number: M00573090
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0775-2022·2022-03-23
Boston Scientific JAGTOME RX device recalled for sterile barrier breach
Boston Scientific has recalled 2209 units of the JAGTOME RX medical device worldwide due to compromised sterility from a sterile barrier breach. The affected units were distributed across the US and more than 40 countries.
Product
JAGTOME RX 44-30-260-035 Material Number: M00573060
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0807-2022·2022-03-23
BioPlex 2200 Syphilis Calibrator Set Recall Due to Vaccine Interference and Reagent Stability Issues
Bio-Rad Laboratories is recalling 724 BioPlex 2200 Syphilis Calibrator sets due to COVID-19 vaccine interference concerns and manufacturing problems with reagent stability. The recalled lots were distributed nationwide in the U.S. and internationally.
Product
BioPlex 2200 REF 12000651 Syphilis Total & RPR Calibrator Set CAL
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0869-2022·2022-03-23
Honey BBQ seasoning recalled due to undeclared wheat allergen
PS Seasoning & Spices recalls Honey BBQ Snack seasoning (3,001 units) distributed to 28 states and Canada due to undeclared wheat. Consumers with wheat allergies should not use affected lots.
Product
Honey BBQ Snack, NO MSG Seasoning packaged in the following sizes: 1. 685-A, Net Wt 21 lbs. (9.52kg). Part #020001456. 2. 685-B, Net Wt 5.25 lbs. (2.38kg). Part #020001457. Ingredients: Sugar, Salt, Dried Honey, Spices, Brown Sugar, Onion and Garlic Powder…
Category
Food
Distribution
27 states
HighFDA (Devices)·Z-0795-2022·2022-03-23
Lumbar Puncture Tray Adult recalled due to manometer failure and leaking
Bard Peripheral Vascular Inc is recalling 8,630 lumbar puncture trays due to manometer failure causing leaking and mating issues. Devices were distributed nationwide in the U.S. plus Puerto Rico, Costa Rica, and Hong Kong.
Product
LUMBAR PUNCTURE TRAY ADULT 18G X 3.5
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0892-2022·2022-03-23
Plant-Based Chicken Chipotle Pasta Salad Kit Recalled for Plastic Contamination
Fresh Creative Foods is recalling Plant Based Chicken Chipotle Pasta Salad Kit due to hard plastic pieces found in the product. The plastic contamination came from ice purchased from a supplier.
Product
Fresh Creative Foods PLANT BASED CHICKEN CHIPOTLE PASTA SALAD KIT 2/5.8125 LB UPC: 10013454381820 Item # 404996 Kit Components: 2/4.5 lb. tubs of Chipotle Pasta Salad; 2/15 oz. bags of plant based chipotle seasoned protein strips 2/5 oz. bags of shredded cheddar cheese…
Category
Food
Distribution
20 states
HighFDA (Food)·F-0893-2022·2022-03-23
Basil Pesto Bowtie Pasta Salad Kits Recalled for Hard Plastic Contamination
Fresh Creative Foods is recalling Basil Pesto Bowtie Pasta Salad Kits because hard clear plastic pieces were found in the product during manufacturing. The plastic originated from ice purchased from the manufacturer's supplier.
Product
Fresh Creative Foods; BASIL PESTO BOWTIE PASTA SALAD DIRECT KIT 2/5.15625 LB UPC: 10013454380922; Item # 404736 Perishable/ Keep Refrigerated Kit components: 2/3 lb. bags of Bowtie Pasta, 2/24 oz. bags of Sweet Basil Dressing, 2/8 oz. bags of diced sundried tomato, 2/2.5 bags…
Category
Food
Distribution
20 states
HighFDA (Devices)·Z-0791-2022·2022-03-23
Lumbar Puncture Tray Pediatric Recalled Due to Manometer Failure
Bard Peripheral Vascular Inc is recalling pediatric lumbar puncture trays due to manometer leaking and mating failures that could prevent proper pressure measurement during procedures.
Product
LUMBAR PUNCTURE TRAY PEDIATRIC 21G 2.5
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0781-2022·2022-03-23
Boston Scientific RX Cholangiogram Kit Recall Due to Sterile Barrier Breach
Boston Scientific is recalling RX Cholangiogram Kits because the sterile barrier has been breached, compromising the sterility of the devices. The affected kits were distributed worldwide.
Product
RX CHOLANGIOGRAM KIT - SINGLE Material Number: M00575240 M00575240 M00575280 M00575320 M00575360 M00575380 M00575400 M00575440 M00575480
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0766-2022·2022-03-23
Boston Scientific recalls 68 medical devices with sterility breach
Boston Scientific is recalling 68 JAGTOME REVOLUTION RX medical devices due to sterile barrier breach. The devices were distributed worldwide including throughout the US.
Product
JAGTOME REVOLUTION RX 39-20-450-025 Material Number: M00584250
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0762-2022·2022-03-23
HYDRATOME RX surgical device recalled due to sterile barrier breach
Boston Scientific recalls 251 HYDRATOME RX 44-30MM/450CM units worldwide due to sterile barrier breach that compromises device sterility.
Product
HYDRATOME RX 44-30MM/450CM Material Number: M00583070
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0790-2022·2022-03-23
FDA Recalls Safe-T PLUS Pediatric Lumbar Puncture Tray Due to Manometer Failure
Bard Peripheral Vascular Inc is recalling 20,400 Safe-T PLUS pediatric lumbar puncture trays due to manometer leaking and mating failures. The devices were distributed nationwide and internationally to healthcare facilities.
Product
Safe-T PLUS Pediatric/Infant Lumbar Puncture Tray, 22 g x 1.5" Spinal Needle with Manometer
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0771-2022·2022-03-23
Medical Device Recall: Boston Scientific JAGTOME RX Sterile Barrier Breach
Boston Scientific is recalling 98 units of the JAGTOME RX 39-30-260-025 medical device due to compromised sterile barrier that affects device sterility. Units were distributed worldwide.
Product
JAGTOME RX 39-30-260-025 Material Number: M00573100
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0778-2022·2022-03-23
Boston Scientific JAGTOME RX Recalled for Sterile Barrier Breach
Boston Scientific is recalling 96 units of JAGTOME RX medical devices due to a sterile barrier breach that compromises device sterility. Patients should contact their physician if they received this device.
Product
JAGTOME RX 49-30-260-035 Material Number: M00573020
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-0891-2022·2022-03-23
Broccoli Cheddar Pasta Salad Recalled Due to Hard Plastic Contamination
Walmart's Freshness Guaranteed Broccoli Cheddar Pasta Salad is recalled due to hard plastic pieces found during manufacturing. The contamination came from ice purchased from a supplier and affects products with use-by dates of March 14–22, 2022.
Product
Freshness Guaranteed BROCCOLI CHEDDAR PASTA SALAD WM 6/14 OZ (397 g) UPC: 0 78742 37256 3 Distributed by Walmart Inc., Bentonville, AR 72716
Category
Food
Distribution
20 states
HighFDA (Devices)·Z-0776-2022·2022-03-23
Medical Device Sterile Barrier Breach: JAGTOME RX Recall
Boston Scientific is recalling JAGTOME RX medical devices because the sterile barrier may be compromised, which could allow contamination. The recall affects 163 units distributed worldwide.
Product
JAGTOME RX 44-30-450-035 Material Number: M00573070
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0788-2022·2022-03-23
LYFO Disk Quality Control Product Recalled for Organism Mislabeling
Microbiologics Inc recalls LYFO Disk lot 983-40-3 because it is labeled as Candida tropicalis but actually contains Yersinia enterocolitica. The mislabeling may cause laboratory quality control failures and delayed test results.
Product
LYFO Disk
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0805-2022·2022-03-23
Calcium Alginate Wound Dressings Recalled for Incorrect Instructions
CellEra LLC is recalling Vitale Silver calcium alginate dressings nationwide because packages contain incorrect Instructions for Use with language not approved by the FDA. The firm is providing replacement packages with corrected instructions.
Product
20548 Vitale Silver calcium Alginate Dressings 4x8, 5/box
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0870-2022·2022-03-23
Seasoning Recall: Undeclared Wheat in Honey BBQ Snack Stick Seasoning
PS Seasoning & Spices, Inc. recalled Honey BBQ Snack Stick Seasoning containing undeclared wheat, affecting approximately 10,441 units distributed across multiple U.S. states and Canada. Consumers with wheat allergies should not consume affected products.
Product
Honey BBQ Snack Stick Seasoning packaged in the following sizes: 1. 765-A, Net Wt 21 lbs. (9.52kg). Part #020001203. 2. 765-B, Net Wt 5.25 lbs. (2.38kg). Part #020001299. 3. 765-C, Net Wt 2.63 lbs (1.19kg). Part #020001513. Ingredients: Sugar, Salt, Dried…
Category
Food
Distribution
27 states