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 Sep 13, 2021
SAS Foods Enterprises Inc. Recalls Frozen, Fully Cooked Beef and Chicken Empanada Products Packaged without Benefit of…
High riskUsing this product could cause serious injury, illness or death — stop using it now.SAS Foods Enterprises Inc.
USDA FSIS
Reported Sep 8, 2021
TRUMATCH CT PIN GUIDE KIT L- TruMatch Patient Specific Instruments are intended to be used as patient-specific surgical…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.DePuy Orthopaedics, Inc.
6 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 8, 2021
Hostess Soft White Hamburger Buns, Net Wt. 12 OZ, UPC 888109110987
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Hostess Brands, LLC
1 more product in this recall
FDA (openFDA food enforcement)
Reported Sep 8, 2021
Strawberry Yogurt Granola Parfait packaged in clear plastic cups and labeled in the following ways: 1) Go Fresh Market…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Loffredo Fresh Gardens Inc. dba Produce Innovations
2 more products in this recall
FDA (openFDA food enforcement)
Reported Sep 8, 2021
Gyrus Acmi PKS Omni 5mm/33cm-intended for the electrosurgical coagulation, mechanical grasping, and dissection of…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Olympus Corporation of the Americas
FDA (openFDA device enforcement)
Reported Sep 8, 2021
Artis Models with SW version VD12 listed below: Artis zee floor 10094135 Artis zee ceiling 10094137 Artis zee MP…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Sep 8, 2021
CoolSculpting Elite System The CoolSculpting System SW release 2.0, SW release 3.0, SW release 3.0.1, SW release 3.0.2
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zeltiq Aesthetics, Inc.
FDA (openFDA device enforcement)
Reported Sep 1, 2021
AUGMENT Injectable Kit, 3cc, Model K30003010, Lot 1706343
Moderate riskThis product could cause temporary or reversible health problems — stop using it.BioMimetic Therapeutics, LLC
FDA (openFDA device enforcement)
Reported Sep 1, 2021
Monoject 0.9% Sodium Chloride Flush Syringe, 10 mL Fill, STERILE, Product Code 8881570121 The proposed device is…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Cardinal Health
2 more products in this recall
FDA (openFDA device enforcement)
Reported Sep 1, 2021
AltiVate Anatomic Shoulder System for the following Part Numbers: 1. Part # 520-08-00, Rev. C., 2. Part # 520-10-000,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Encore Medical, LP
FDA (openFDA device enforcement)
Reported Sep 1, 2021
Crunchmaster Multi Grain Baked Gluten-Free Crackers 5-Seed Sesame, Amaranth, Flax, Chia & Quinoa 20 oz. UPC Code:…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.TH Foods Inc.
FDA (openFDA food enforcement)
Reported Sep 1, 2021
Gore Molding & Occlusion Balloon Catheter, REF Catalogue Number MOB37, SN XXXXXXXX, 10 mm - 37 m 10 Fr, Guidewire…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.W. L. Gore & Associates Inc.
FDA (openFDA device enforcement)
Reported Aug 25, 2021
DELTAVEN Safety I.V. Catheter in Pur with closed system: a) REF 3836272 b) REF 3814272 c) REF 3845272 d) REF 3856272
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Delta Med SpA
10 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 25, 2021
Triathlon Prim CEM FXD BPLT 7, Catalog No. 5520B700
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Howmedica Osteonics Corp.
FDA (openFDA device enforcement)
Reported Aug 25, 2021
Flavored Bacon Ranch Seasoning Packaged in 25lb kraft paper bags
High riskUsing this product could cause serious injury, illness or death — stop using it now.Mane Inc.
2 more products in this recall
FDA (openFDA food enforcement)
Reported Aug 25, 2021
FLASH Ostial System, Dual Balloon Angioplasty Catheter, REF: OAB6014BA
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ostial Corporation
FDA (openFDA device enforcement)
Reported Aug 25, 2021
728306 Brilliance iCT-Computed Tomography X-ray systems 728305 Brilliance iCT Upgrades
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips North America LLC
4 more products in this recall
FDA (openFDA device enforcement)
Reported Aug 25, 2021
EPIQ Ultrasound Systems, Model: EPIQ Elite, EPIQ 5G, EPIQ 5C, EPIQ 5W, EPIQ 7G, EPIQ 7C, EPIQ 7W, EPIQ CVx, EPIQ CVxi
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Philips Ultrasound Inc.
FDA (openFDA device enforcement)
Reported Aug 25, 2021
The Aequalis Pyrocarbon Humeral Heads. Shoulder implant component. Sold OUS only: a) Catalog # DWH039 - Diameter 39 mm…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Tornier S.A.S.
FDA (openFDA device enforcement)
Reported Aug 18, 2021
Kaluza C Flow Cytometry Software Versions: 1.0*, 1.1.1 and 1.1.2 Kits: C10574 - Kaluza C Single Perpetual License…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Beckman Coulter, Inc.
FDA (openFDA device enforcement)
Reported Aug 18, 2021
ETEST IMIPENEM RELEBACTAM. in vitro diagnostic
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Biomerieux Inc.
FDA (openFDA device enforcement)
Reported Aug 18, 2021
Chassis Label - "CIRRUS HD-OCT Rx-Only" Product Label Exterior RX - "CIRRUS HD-OCT Model 6000"
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Carl Zeiss Meditec, Inc.
FDA (openFDA device enforcement)
Reported Aug 18, 2021
Covidien Sonicision Reusable Generator-converts electrical power from the battery pack to ultrasonic energy to drive…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Covidien LLC
FDA (openFDA device enforcement)
Reported Aug 18, 2021
Solumeve Hydrolyzed Collagen Peptides, Turmeric + MCT and Ginger; Dietary Supplement, NET Wt. 14.1 oz. (400g) Suggested…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Iherb LLC
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.