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.
Reported May 20, 2026
Codman CerebroFlo EVD Catheter with Endexo Technology. Contains 5 sets. Product ID: 37.550.501. The CerebroFlo EVD…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp. (NeuroSciences)
FDA (openFDA device enforcement)
Reported May 20, 2026
LUCAS 2 Model Number: 99576 Catalog Numbers: 99576-000024 and 99576-000011 UDI-DI code: 00883873904565 LUCAS 3 Model…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Jolife AB
FDA (openFDA device enforcement)
Reported May 20, 2026
QuickVue Dipstick Strep A Test, 50T, REF 20108, antigens, all groups, streptococcus spp.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Quidel Corporation
FDA (openFDA device enforcement)
Reported May 20, 2026
Diowave Laser System, REF: Diowave 250W
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Technological Medical Advancements LLC
FDA (openFDA device enforcement)
Reported May 13, 2026
Convenience kits containing Medline Namic Angiographic Control Syringes with Rotating Adaptor CORONARY ANGIO PACK Model…
High riskUsing this product could cause serious injury, illness or death — stop using it now.American Contract Systems Inc.
FDA (openFDA device enforcement)
Reported May 13, 2026
ERBEFLO CleverCap CO2: Hybrid CO2 Tubing/Cap Set for Olympus Scopes & CO2 Sources, REF: 20325-239; Hybrid CO2…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Erbe Medical, LLC
2 more products in this recall
FDA (openFDA device enforcement)
Reported May 13, 2026
french broad CHOCOLATE bette's bake sale (a multi-flavor bonbon assortment). 6-piece NET WT. 2.5 OZ (70.75G); 12-piece…
High riskUsing this product could cause serious injury, illness or death — stop using it now.French Broad Chocolate Factory
FDA (openFDA food enforcement)
Reported May 13, 2026
Intuitive 8 mm SureForm 30 Gray Reloads Reference Numbers: 48230M-05 and 48230M-06
High riskUsing this product could cause serious injury, illness or death — stop using it now.Intuitive Surgical, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported May 13, 2026
LIFEPAK 15, REF: 99577-000025, 99577-000047, 99577-001256, 99577-001217, 99577-001241, 99577-001255, 99577-001219,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Physio-Control, Inc.
FDA (openFDA device enforcement)
Reported May 13, 2026
Good & Gather Fresh from Our Deli. Sesame Teriyaki Chicken with Rice. Net Wt 18.0 oz (1.125lb). Keep Refrigerated. DPCI…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Target Corporation
FDA (openFDA food enforcement)
Reported May 6, 2026
Brand Name: HiResolution" Bionic Ear System Product Name: M Zn-Air Battery Pak Model/Catalog Number: CI-5501-110;…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Advanced Bionics, LLC
FDA (openFDA device enforcement)
Reported May 6, 2026
Brand Name: Kiwi Omni Vacuum Delivery System Product Name: Kiwi Omni Vacuum Delivery System Model/Catalog Number:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Clinical Innovations, LLC
FDA (openFDA device enforcement)
Reported May 6, 2026
Depuy Synthes, ATTUNE REVISION HINGE FEMORAL LT SZ 4 CEM. Part Number: 150450104.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Depuy (ireland)
8 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 29, 2026
LSL Healthcare, Central Line Dressing Kit, Model/Catalog Number: 2717H
Moderate riskThis product could cause temporary or reversible health problems — stop using it.LSL Healthcare Inc.
5 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 29, 2026
Bulk Horchata Powder 3951 (100547) 1/25 HORCHATA UPC: 042743-19015-0 Item: 100547
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Marquez Brothers International, Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Apr 29, 2026
CHIPS AHOY! Baked Bites Brookie .22.4 oz Carton ( 2.8 oz pouch ) and 7.7 oz Carton ( 1.4 oz pouch)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mondelez Global LLC
FDA (openFDA food enforcement)
Reported Apr 29, 2026
Oxoid Agglutinating Sera, Salmonella 9-0 R30957301
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Remel Europe Ltd.
FDA (openFDA device enforcement)
Reported Apr 29, 2026
Flamingo Funnel Small, Model Number SQ20012-01
Moderate riskThis product could cause temporary or reversible health problems — stop using it.SurgiSmoke Solutions
2 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 22, 2026
iLet Ace Pump Kit REF: BB1001 iLet Dosing Decision Software
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beta Bionics, Inc.
FDA (openFDA device enforcement)
Reported Apr 22, 2026
Gentuity HF-OCT Imaging System Model G10-01; Software version 23.2.13;
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Gentuity, LLC
FDA (openFDA device enforcement)
Reported Apr 22, 2026
Cytal Wound Matrix 2-Layer 5x5 cm. Product ID: WSM0505.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Integra LifeSciences Corp. (NeuroSciences)
4 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 22, 2026
Philips Spectral CT on Rails. Model Number: 728334.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Medical Systems
FDA (openFDA device enforcement)
Reported Apr 22, 2026
Instinct Plus Endoscopic Clipping Device REF: G58010 Rx Only, Sterile EO
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Wilson-Cook Medical Inc.
FDA (openFDA device enforcement)
Reported Apr 15, 2026
Vital Nutrients Aller-C (vitamin C, citrus bioflavonoids, isoquercitrin, and bromelain)100 count bottles and 200 count…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Blueroot Health, Inc.
FDA (openFDA food 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.