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 3, 2021

Infusion Pump

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

Baxter Healthcare Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Mar 3, 2021

VITROS Chemistry Products VersaTips - Product Usage: used to dispense samples to MicroSlide assays and sample and…

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

Ortho-Clinical Diagnostics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 3, 2021

PHILIPS BATTERY, V60 14.4V, 11.0 Ah, 163 Wh, REF 1076374(1058272), LOT M94663-P1 - Product Usage: The ventilator is…

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

Respironics California, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Mar 3, 2021

ENROUTE Transcarotid Stent System REF SR-XXYY-CS

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

Silk Road Medical Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 3, 2021

Tube Tracheostomy and Tube Cuff, Bivona¿ Cuffless Neonatal/Pediatric FlexTend" Tracheostomy Tube (model 60PFS45, lots…

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

Smiths Medical ASD Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Mar 3, 2021

OT1000 Series Orthopedic Surgical Tables

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

Steris Corporation

FDA (openFDA device enforcement)

Meat & poultry

Reported Feb 26, 2021

J&J Distributing Recalls Ready-to-Eat Meat and Poultry Salads and Wrap Products Due to Possible Listeria Contamination

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

J&J Distributing

USDA FSIS

Meat & poultry

Reported Feb 25, 2021

FSIS Issues Public Health Alert for Beef Meatball Products Due to Misbranding and Undeclared Allergen

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

Fsis

USDA FSIS

Food

Reported Feb 24, 2021

20 Mile Black Cherry Organic Frozen Custard, Contents: One U.S. Pint, and 86 oz. Scoopers. UPC 50005-48807. Made by…

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

Barron County Organics

16 more products in this recall

FDA (openFDA food enforcement)

Medical devices

Reported Feb 24, 2021

Central Screw 6.5x25mm - Product Usage: used as a sterile screw that is intended for implantable shoulder prosthesis…

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

Biomet, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 24, 2021

Healgen COVID-19 IgG/IgM Rapid Test Cassette (Whole Blood/Serum/Plasma) REF GCC)V-402a - Product Usage: is a lateral…

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

Confirm Biosciences Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 24, 2021

Getinge CM320 Series Washer Disinfector - Product Usage: A multi chamber washer disinfector intended for washing,…

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

Getinge Group Logistics America, LLC

FDA (openFDA device enforcement)

Medical devices

Reported Feb 17, 2021

Argon Medical Devices TLAB, Transjugular Liver Biopsy System, REF: TL - 18S, 1/18 GA Flexcore Biopsy Needle, 1/7F…

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

Argon Medical Devices, Inc.

5 more products in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 17, 2021

Arjo Flat Dynamic Positioning System (DPS) - Product Usage: used in conjunction with passive clip slings is designed…

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

Arjohuntleigh Magog, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 17, 2021

Aquarius LPH 511-A CRLF2 Distal Probe Green, model no. LPH 511-A The CRLF2 Distal probe, labelled in green, consists of…

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

Cytocell Ltd.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 17, 2021

Universal Femoral Sleeves - Product Usage: used primarily in revision surgeries with the S-ROM Noiles, LPS, SIGMA, and…

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

DePuy Orthopaedics, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 17, 2021

Infinity Acute Care System (IACS) Monitoring Solution: The IACS is intended for multi-parameter, physiologic patient…

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

Draegar Medical Systems, Inc.

FDA (openFDA device enforcement)

Medical devices

Reported Feb 17, 2021

60 IN (152cm) APPX 1.5 ml, PUR YELLOW SMALLBORE SET, FILTER REF B2209 - Product Usage: The intravascular administration…

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

ICU Medical, Inc.

3 more products in this recall

FDA (openFDA device enforcement)

Food

Reported Feb 17, 2021

Kowalski's Buffalo Cauliflower Bites with Kowalski's Steakhouse Blue Dressing. Net Wt. 22 oz (1 lb. 6 oz) 624 g. UPC…

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

Russ Davis Wholesale Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Feb 10, 2021

FLOW COUPLER Monitor Flow Coupler devices are sold in 5 sizes (2.0 mm, 2.5 mm, 3.0 mm, 3.5 mm, 4.0 mm). Implantable…

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

Baxter Healthcare Corporation

FDA (openFDA device enforcement)

Medical devices

Reported Feb 10, 2021

Neuroreader Medical Image Processing Software - Product Usage: intended to automate the current manual process of…

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

Brainreader ApS

FDA (openFDA device enforcement)

Food

Reported Feb 10, 2021

Dole Endless Summer Salad Kit; 13 oz. bag UPC: 0-71430-01073-0 Contains Milk, Wheat Distributed by Dole Fresh…

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

Dole Fresh Vegetables Inc.

FDA (openFDA food enforcement)

Medical devices

Reported Feb 10, 2021

Philips EPIQ Diagnostic Ultrasound System; Model Numbers: EPIQ Elite, EPIQ 5G, EPIQ 5C, EPIQ 7G, EPIQ 7C, EPIQ CVx &…

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

Philips Ultrasound Inc.

1 more product in this recall

FDA (openFDA device enforcement)

Medical devices

Reported Feb 3, 2021

B. Braun Introcan IV Safety Catheters, sterile - Product Usage: It is a single-use device to generate intravascular and…

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

Braxton Medical Corporation

FDA (openFDA device enforcement)

Free recall alerts

Get alerted about new Minnesota recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

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.