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.

3,899 stored notices name Minnesota, reported between Jun 20, 2012 and Nov 11, 2026. A further 48,759 notices were distributed nationwide, so they reach Minnesota too — those are in the archive.

Medical devices

Reported Sep 25, 2024

ERIC Retrieval Device REF: ER173020 ER174030 ER176044 The ERIC Retrieval Device is a mechanical thrombectomy device…

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

Microvention Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 25, 2024

Seer Home System is an ambulatory electroencephalograph (EEG) system intended for at-home use for extended EEG and…

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

Seer Medical Pty Ltd.

FDA (openFDA device enforcement)

Food

Reported Sep 18, 2024

American Outdoor Products - Astronaut Strawberries, packaged in 0.5oz (14g) metallic plastic pouches. Sold individually…

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

American Outdoor Products, Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Sep 18, 2024

FILMARRAY 2.0 INSTRUMENT, REF: FLM2-ASY-0001, FLM2-ASY-0001-W

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

BioFire Diagnostics, LLC

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 18, 2024

Asli Cinnamon Powder, 7oz clear plastic pouch, UPC 703440150723

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

Sands Impex Inc. dba Asli Fine Foods

FDA (openFDA food enforcement)

Medical devices

Reported Sep 18, 2024

Brand Name: Vit-l-escence Product Name: Vit-l-escence Singles A3 Model/Catalog Number: 1203- Software Version: N/A…

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

Ultradent Products, Inc.

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 11, 2024

BD Pyxis QFill Replenishment Station, REF: 138904-01, medication cabinet system

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

CareFusion 303, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Food

Reported Sep 11, 2024

Item 41303.82013, Reser's Essential Everyday Original Potato Salad, refrigerated product, net wt. 16oz. There are 6…

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

Reser's Fine Foods, Inc.

13 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Sep 11, 2024

Heparin, Gore Viabahn VBX, Balloon Expandable Endoprosthesis, for the following Reference numbers: United States:…

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

W L Gore & Associates, Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Sep 4, 2024

FreeStyle Libre 3 Sensors, REF: 72081-01, component of the FreeStyle Libre 3 Continuous Glucose Monitoring System

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

Abbott Diabetes Care, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Sep 4, 2024

Afinion 2 Analyzer, model #1116986, US refurbished, CLIA waived.

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

Abbott Diagnostics Technologies AS

FDA (openFDA device enforcement)

Medical devices

Reported Aug 28, 2024

DxC 500 AU Clinical Chemistry Analyzer, REF C63520 is an automated chemistry analyzer that measures analytes in…

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

Beckman Coulter Mishima K.K.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 28, 2024

McGrath Mac Video Laryngoscope, REF: 300-000-000 , Non-Sterile, Rx Only

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

Covidien

2 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Aug 28, 2024

ClotTriever XL Catheter, 30 mm, REF: 41-102, used with Instructions for Use ClotTriever XL Catheter ClotTriever…

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

Inari Medical - Oak Canyon

FDA (openFDA device enforcement)

Food

Reported Aug 28, 2024

L&B Beautiful Morning Glory Muffins. Product #49025. 4 muffins per container. Net Wt 14 oz. UPC 18169-49025.

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

Lunds Mitchell Rd LLC

FDA (openFDA food enforcement)

Medical devices

Reported Aug 28, 2024

Multiple Digital Analog Products labeled as: NobelBiocare Tri-Lobe-compatible 6.0mm Digital Analog, REF 9000703…

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

Preat Corp.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 28, 2024

Ventana anti-CD10 (SP67) Rabbit Monoclonal Primary Antibody, REF: 790-4506, IVD

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

Ventana Medical Systems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 21, 2024

BD Kiestra Urine Culture Application Powered by BD Synapsys Informatics Solution; Catalog (Ref): 444900;

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

Becton Dickinson & Co.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 21, 2024

WAVEWRITER ALPHA: Model: SC-1216, 16 IPG KIT, REF: M365SC12160; Model: SC-1232, 32 IPG KIT, REF: M365SC12320

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

Boston Scientific Neuromodulation Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Aug 21, 2024

Cepheid, Sample Collection Device, Part: 900-0370

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

Cepheid

FDA (openFDA device enforcement)

Medical devices

Reported Aug 21, 2024

Product Name: Salivary Testosterone ELISA Model/Catalog Number: SLV-3013 Product Description: An enzyme immunoassay for…

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

DRG International, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Aug 21, 2024

Various Merit Medical convenience kits that contain recalled Jiangsu Shenli Medical Production Co. Ltd. syringes: Rapid…

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

Merit Medical Systems, Inc.

22 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Aug 21, 2024

Lunds & Byerlys Fresh Guacamole Dip, Net Wt 14 oz (396g). UPC 0 72431-66072 6. Keep Refrigerated.

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

Metro Produce Distributors, Inc.

4 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Aug 21, 2024

HeartMate 3 System Controllers provided within the following HeartMate 3 Left Ventricular Assist System (LVAS) Implant…

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

Thoratec LLC

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.