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.
Reported Sep 2, 2026Updated Sep 13, 2026
Byron White FORMULAS A-P Herbal Supplement 1.0 fl. oz./30 mL May Contain Nuts (Juglans nigra hull) Byron White Formulas…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Byron White Formulas, Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 2, 2026Updated Sep 7, 2026
Alphenix Models INFX-8000C INFX-8000F INFX-8000V This device is a digital radiography/fluoroscopy system used in a…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Canon Medical System, USA, Inc.
FDA (openFDA device enforcement)
Reported Sep 2, 2026Updated Sep 7, 2026
Outshine Fruit Bar Watermelon, 6-Count 2.5 ounce with UPC 041548413624, packaged in paper outer cartons; individual…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dreyer's Grand Ice Cream Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Sep 2, 2026Updated Sep 16, 2026
Outshine Fruit Bars Strawberry, 6-Count 2.5 ounce, with UPC 041548610047, packaged in paper outer cartons; individual…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Dreyer's Grand Ice Cream Inc.
3 more products in this recall
FDA (weekly enforcement report)
Reported Sep 2, 2026Updated Sep 16, 2026
hodo CHILI CRISP LIGHTLY FRIED TOFU. NET WT 8oz. KEEP REFRIGERATED. Manufactured by: Hodo Inc., Oakland, CA 94608. UPC:…
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Hodo Inc.
FDA (weekly enforcement report)
Reported Sep 2, 2026Updated Sep 16, 2026
IV Sets with drip chambers
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ICU Medical, Inc.
FDA (weekly enforcement report)
Reported Aug 26, 2026Updated Sep 7, 2026
American Contract Systems medical procedure kits and trays labeled as: 1) CRANI PACK - 208400, Model Item Number…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.American Contract Systems Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Aug 26, 2026Updated Sep 7, 2026
BD Needle Kit for Powered Driver 15mm x 15Ga, REF: D015151NK, BD Needle Kit for Powered Driver 25mm x 15Ga, REF:…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Bard Access Systems, Inc.
FDA (openFDA device enforcement)
Reported Aug 26, 2026Updated Sep 7, 2026
Esteem Body Soft Convex Urostomy Pouch Model/Catalog Numbers: 423703, 423704, 423705, 423707, 423708, 423709, 423710,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.ConvaTec, Inc.
FDA (openFDA device enforcement)
Reported Aug 26, 2026Updated Sep 7, 2026
EndoFLIP System that includes: ENDOFLIP 1 SYSTEM EF-100 05391530810050 10884521809307 REFURBISHED SYSTEM RFG-EF100…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien, LLC
FDA (openFDA device enforcement)
Reported Aug 26, 2026Updated Sep 7, 2026
GETINGE Y SENSOR Module, SERVO-U, SERVO-N, Model Number 6693662; part of the SERVO-U/-N continuous ventilator system,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Maquet Critical Care AB
FDA (openFDA device enforcement)
Reported Aug 26, 2026Updated Sep 7, 2026
Paragonix Technologies Inc. KidneyVault Portable Renal Perfusion System REF# PRGNX-8008-001
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Paragonix Technologies Inc.
FDA (openFDA device enforcement)
Reported Aug 26, 2026Updated Sep 7, 2026
Prospector Popcorn Maple Walnut Ice Cream Gourmet Popcorn 3.5 oz.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.Prospector Popcorn, LLC
3 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 26, 2026Updated Sep 7, 2026
Dentsply Sirona Capsule Mixer Model No. 5546068
Moderate riskThis product could cause temporary or reversible health problems — stop using it.SDI Limited
FDA (openFDA device enforcement)
Reported Aug 26, 2026Updated Sep 7, 2026
Whole Foods Medium Pico de Gallo Guacamole Dip, Keep Refrigerated. Packed in various sized clear plastic containers.…
High riskUsing this product could cause serious injury, illness or death — stop using it now.WFM Purchasing, LP
9 more products in this recall
FDA (openFDA food enforcement)
FoodReported Aug 22, 2026
Everything Sprouts, LLC Recalls Alfalfa Sprouts Due to Potential E. Coli and Salmonella Risk
Risk not classifiedThe agency has not ranked the risk yet — treat the notice as a caution.Everything Sprouts, LLC
FDA (recalls & safety alerts)
Reported Aug 19, 2026Updated Sep 7, 2026
Aquafaba Powder, Vegan Replacement, NET WT. 4 oz (113g) and 12 0z (340g), Resealable stand-up matte foil pouch with…
High riskUsing this product could cause serious injury, illness or death — stop using it now.529 Commerce, LLC
FDA (openFDA food enforcement)
Reported Aug 19, 2026Updated Aug 25, 2026
60 In Non-DEHP Minibore Extension Set RES ME2010 UDI-DI code: 10885403236235 MaxPlus Ext Set w/Needleless and Y-Site…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Bd Switzerland Sarl
FDA (openFDA device enforcement)
Reported Aug 19, 2026Updated Aug 25, 2026
BIOFIRE Respiratory Panel 2.1 (RP2.1) REF 423742 UDI code: 00815381020529 PCR-based multiplexed nucleic acid test, in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioFire Diagnostics, LLC
FDA (openFDA device enforcement)
Reported Aug 19, 2026Updated Sep 7, 2026
ERBECRYO 2 Cryosurgical Unit Model/Catalog Number: 10402-000
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Erbe USA Inc.
FDA (openFDA device enforcement)
Reported Aug 19, 2026Updated Aug 25, 2026
Boston Scientific Enhance Transcarotid/Peripheral Access Kit REF: SR-4F21G7D-MP (Kit-075-03) Sheath with Dilator ,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Galt Medical Corporation
FDA (openFDA device enforcement)
Reported Aug 19, 2026Updated Aug 25, 2026
BOBBY Balloon Guide Catheter REF: BOB-895-CN BOB-895-EMEA BOB-895-EMEA-AL BOB-895-US MV-BGA01095 For use in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Microvention Inc.
FDA (openFDA device enforcement)
Reported Aug 19, 2026Updated Sep 16, 2026
Red Blood Cells, Leukocytes Reduced
Moderate riskThis product could cause temporary or reversible health problems — stop using it.New York Blood Center Inc.
FDA (weekly enforcement report)
Reported Aug 19, 2026Updated Aug 25, 2026
OBP Medical , ER-Spec Single-Use Vaginal Speculum with LED Light Source, X-Small REF: C020130-1
Moderate riskThis product could cause temporary or reversible health problems — stop using it.OBP Medical Corporation
FDA (openFDA device enforcement)
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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.