All recall categories

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.

3,845 stored notices name Minnesota, reported between Jun 20, 2012 and Sep 23, 2026. A further 48,100 notices were distributed nationwide, so they reach Minnesota too — those are in the archive.

Medical devices

Reported Mar 5, 2025

IntelePACS (Image Fusion Module) - InteleViewer

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

Intelerad Medical Systems Incorporated

FDA (openFDA device enforcement)

Food

Reported Mar 5, 2025

Gerber Snacks for Baby Soothe 'n' Chew TEETHING STICKS Strawberry Apple NET WT 3.2 OZ (90g) UPC 0 15000 04518 7 GERBER…

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

Nestle-USA, Inc. (Corporate Office)

1 more product in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Mar 5, 2025

Socrates 38 Aspiration Catheter 127 cm length REF SC038-127-001 The Socrates Aspiration System with a compatible…

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

Scientia Vascular, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 26, 2025

DeRoyal AMG Suction Connector Tubing REF: 71-2083, 71-C506, 71-C510, 71-C512, 71-C520, Tubing is intended for fluid…

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

DeRoyal Industries Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 26, 2025

Dexcom G6, Continuous Glucose Monitoring System, REFs: STK-OM-001, STR-OM-001, STR-OR-001

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

Dexcom, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 26, 2025

Jack & the Green Sprouts Alfalfa Sprouts. Net Weight 5 oz. (152g). UPC 7 63247-19891 5. Keep Refrigerated. Product of…

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

Jack & The Green Sprouts, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Feb 26, 2025

3M Prevena Plus 125 Therapy Unit and System Kits REF: PRE3021US Prevena Plus Duo Peel and Place 20cm System Kit, US…

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

Kci USA, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 19, 2025

AcuMatch XLE Item Number / Product Description: 140-28-27 AM EHXL 0¿ LNR G 28MM 140-32-27 AM EHXL 0¿ LNR G 32MM…

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

Exactech, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 19, 2025

Pearl Milling Company Original Pancake & Waffle Mix 32 OZ (2LB) 907g 30000 65040 BBD SEP 13 25 P

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

Frito-Lay, Inc. Headquarters

FDA (openFDA food enforcement)

Medical devices

Reported Feb 19, 2025

Biological, Bio52 HealthFirst Mail In Monitoring System, 52 Tests, Item: 1003600. Biological, Bio12 HealthFirst Mail In…

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

HF Acquisition Co. LLC

FDA (openFDA device enforcement)

Medical devices

Reported Feb 19, 2025

Brand Name: MediHoney¿ Gel Product Name: MediHoney¿ Wound & Burn Dressing Gel Model/Catalog Number: 31815 Software…

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

Integra LifeSciences Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 19, 2025

Max Mobility/Permobil Smart Drive MX2+ SpeedControl Dial Ref: MX2-3DC use in conjunction with the SmartDrive MX2+…

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

Max Mobility LLC

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 12, 2025

Temporary Titanium Abutments

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

DDS Lab

FDA (openFDA device enforcement)

Medical devices

Reported Feb 12, 2025

PROLENE Polypropylene Suture, REF: EH7585H, 8706H, 8833H, 8963H, 8935H PROLENE Suture is indicated for use in general…

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

Ethicon, LLC

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 12, 2025

The Rapid fFN Specimen Collection Tube (PN: 71550-001) is a component of the Rapid fFN Specimen Collection kit (PN:…

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

Hologic, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 12, 2025

SenTiva, REF: 1000; SenTiva Duo, REF: 1000-D; Generators Part of the VNS Therapy System. Used for Vagus Nerve…

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

LivaNova USA, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 12, 2025

UNiD" Adaptive Spine Intelligence UNiD Spine Analyzer Product Number SW3002 UDI-DI code 03613720286929 Two cloud-based…

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

Medicrea International

FDA (openFDA device enforcement)

Medical devices

Reported Feb 12, 2025

NeiMed NasoGel for DRY NOSES UDI-DI/UPC code: 00705928045309 SKU GSP30-2R-48-ENU-USL GSP30-0R-96-ENU-USL GSP30-ARA-INTL…

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

Neilmed Pharmaceuticals Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 12, 2025

Integra Miltex CryoSolutions Cartridges 10 Pack (23.5g N2O each), Model: C-CA-23, Item: 33516;

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

New Medical Technologies GmbH

1 more product in this recall

FDA (openFDA device enforcement)

Meat & poultry

Reported Feb 12, 2025

FSIS Issues Public Health Alert for Frozen Ready-To-Eat Meat and Poultry Pasties Due to Misbranding and Undeclared…

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

The Pasty Oven, Inc.

USDA FSIS

Medical devices

Reported Feb 5, 2025

Calibrate CCX Interbody System for spinal fusion procedures: Implants: (1) Calibrate CCX-O, 7 x 10 x 25mm 5 degrees,…

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

Alphatec Spine, Inc.

FDA (openFDA device enforcement)

Food

Reported Feb 5, 2025

WESTCO 3065 GOLDEN BAVARIAN CREME FILLING ARTIFICIALLY FLAVORED Ingredients: Water, Sugar, Modified Food Starch,…

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

BakeMark USA LLC.

FDA (openFDA food enforcement)

Medical devices

Reported Feb 5, 2025

BD Pyxis MedStation ES AUX Tower REF 343 BD Pyxis " MedStation 4000 AUX Tower REF 314 The BD Pyxis" MedStation ES and…

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

CareFusion 303, Inc.

FDA (openFDA device enforcement)

Food

Reported Feb 5, 2025

Corfu Tzatziki sauce packaged in half gallon plastic tubs, 4 tubs per case. Mediterranean Tzatziki sauce packaged in…

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

Corfu Tasty Gyros

FDA (openFDA food 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.