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Recalls distributed in Minnesota

These notices name Minnesota in the distribution list the company gave its agency. That list says where the product was shipped, not where it ended up — a recalled item can travel with a shopper, and some notices list no states at all.

3,899 stored notices name Minnesota, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,743 notices were distributed nationwide, so they reach Minnesota too — those are in the archive.

Food

Reported Sep 30, 2026Updated Oct 7, 2026

Reese's Crunchy Peanut Ice Cream Bar, 2.0 fl. oz. ice cream bars, paper cartons containing individually wrapped ice…

Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.

Unilever North America Supply Chain Company, LLC

FDA (weekly enforcement report)

Food

Reported Sep 30, 2026Updated Oct 6, 2026

Light Brown Sugar, Packaged in he follow configurations: 1. United, Net Wt. 50 lbs., (22.68kg). Item Number 810051.…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

United Sugar Producers and Refiners

FDA (openFDA food enforcement)

Medical devices

Reported Sep 23, 2026Updated Sep 29, 2026

Power-Trialysis Short-Term Straight Dialysis Catheter, REF: 5605150; Power-Trialysis Short-Term Straight Dialysis…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Bard Access Systems, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 23, 2026Updated Sep 29, 2026

BD Alaris Pump Infusion Sets 10561554* 10885403232565 50885403232563 BD Alaris Pump Infusion Set, 15 Micron Filter,…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Bd Switzerland Sarl

FDA (openFDA device enforcement)

Medical devices

Reported Sep 23, 2026Updated Sep 29, 2026

Boston Scientific Corporation StoneSmart Connect Console Contents: (1) Power Cord, (1) Power Adaptor, (1)DVI Cable, (1)…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Boston Scientific Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Sep 23, 2026Updated Sep 29, 2026

EWO_02512 (Catalog number 320550) For Investigational Use Only Nano Pro Un-Cannulated Demo Samples Quantity 100

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

embecta Medical II LLC

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 23, 2026Updated Sep 29, 2026

Everything Sprouts and Calco branded Alfalfa Sprouts, Net Wt. 5.0 oz (142 g) UPC 7 68944-00005 9. The 5 oz. containers…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Everything Sprouts, LLC

3 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Sep 23, 2026Updated Sep 29, 2026

Happiest Baby, Inc SNOO Sleep Sack, X-Small Model/Catalog Number: S2101-101 S2101-108-6 S2101-133 S2102-112 S2107-101…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Happiest Baby, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 23, 2026Updated Sep 29, 2026

Plum administration sets

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

ICU Medical, Inc.

8 more products in this recall

FDA (openFDA device enforcement)

Drugs

Reported Sep 23, 2026

Red Blood Cells, Leukocytes Reduced

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Innovative Blood Resources

FDA (weekly enforcement report)

Medical devices

Reported Sep 23, 2026Updated Sep 29, 2026

Philips Patient Information Center iX REF:866389

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Philips North America

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 23, 2026Updated Sep 29, 2026

REF:2B5ST Ethicon Endo-Surgery, Inc. XCEL BLADELESS TROCAR W/OPTIVIEW TECHNOLOGY & SLEEVE 5MM X 75MM

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Stryker Sustainability Solutions

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 23, 2026Updated Sep 29, 2026

Rice & Bean Burrito. Ingredients: Rice, Refried Beans, Black Beans, Flame Roasted Corn, Pico De Gallo, Cheese. Net Wt:…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Taylor Fresh Foods Inc.

24 more products in this recall

FDA (openFDA food enforcement)

Food

Reported Sep 23, 2026Updated Sep 29, 2026

Hexing Haw Balls candy; packaged in 200g/0.44 lb./7.05 oz clear plastic bag; Ingredients: haw, white sugar, water.;…

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

Tiffany Food Corp.

FDA (openFDA food enforcement)

Medical devices

Reported Sep 23, 2026Updated Sep 29, 2026

Brand Name: HEMOSPRAY ENDOSCOPIC HEMOSTAT Product Name: HEMOSPRAY ENDOSCOPIC HEMOSTAT Model/Catalog Number: HEMO-7,…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Wilson-Cook Medical Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 16, 2026Updated Sep 22, 2026

Products that contain the Pericare Wipes: Bardex Lubricath Foley Catheter Tray REF: 899914 899916 899918 UDI codes:…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

C.R. Bard Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 16, 2026Updated Sep 22, 2026

HeartSine SAM 350P 350P US Device, US English - 2 Min CPR UDI-DI codes: 0506016712067 350P US Device, US English…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

HeartSine Technologies Ltd.

FDA (openFDA device enforcement)

Food

Reported Sep 16, 2026Updated Sep 22, 2026

Alfalfa, Net Weight 50 lbs. bag, Product of USA, International Specialty Supply 1011 Volunteer Dr. Cookeville, TN 38506

High riskUsing this product could cause serious injury, illness or death — stop using it now.

International Sprout Holdings, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Sep 9, 2026Updated Sep 14, 2026

Halyard medical convenience kits labeled as: 1) ENT, Model/Item Number (kit) ACEN89-01; 2) ENT, Model/Item Number (kit)…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

AVID Medical, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 9, 2026Updated Sep 14, 2026

Baxter Novum IQ Syringe Pump, Model Number 40800BAXUS

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Baxter Healthcare Corporation

20 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 9, 2026Updated Sep 27, 2026

5008X Standard HD Pre-Flush Standard Blood Tubing Set Part Number 03-5110-6

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Fresenius Medical Care Renal Therapies Group, LLC

6 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 9, 2026Updated Sep 14, 2026

HEALON EndoCoat PRO, REF: 10300012 (US/CAN) HEALON DUET PRO II, REF: 10300016 (US/CAN) HEALON EndoCoat PRO, REF:…

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Johnson & Johnson Surgical Vision, Inc.

FDA (openFDA device enforcement)

Food

Reported Sep 9, 2026Updated Sep 16, 2026

Food to Live brand Organic Supergreens mix (kale, moringa leaf, wheat grass, & spirulina), 8 oz, 1 lb, 1.5 lb, 3 lb, 6…

High riskUsing this product could cause serious injury, illness or death — stop using it now.

Lexunder Inc.

FDA (weekly enforcement report)

Medical devices

Reported Sep 9, 2026Updated Sep 14, 2026

Velys Enabling Tech Robotic-Assist Station REF: 451611001

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

Medos International Sarl

FDA (openFDA device enforcement)

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Other states

RecallNow is not a government agency. Every notice above was published by the FDA, USDA FSIS or CPSC and links back to its source. Browse the whole archive.