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 48,122 notices were distributed nationwide, so they reach Minnesota too — those are in the archive.
Reported Apr 13, 2016
Persona The Personalized Knee System Articular Surface Posterior Stabilized (PS) Left Height 14mm Sterile. For use in…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Manufacturing B.V.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 6, 2016
The Spectra-System Dental Implant 2008 system is comprised of dental implant fixtures and prosthetic devices that…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Implant Direct Sybron Manufacturing, LLC
FDA (openFDA device enforcement)
Reported Apr 6, 2016
Jack and the Green Sprouts, Alfalfa Sprouts, Net Wt 5 oz (142 g), UPC 7 6324719891 5 Retail: 5 oz clam shell (cup) .…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Jack And The Green Sprouts, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Apr 6, 2016
Pistachio Raw Whole Shelled 9-oz. retail plastic tub or 5-lb. bulk plastic bag. 12, 9-oz tubs per case. 1, 5# bag per…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Lipari Foods, Inc.
1 more product in this recall
FDA (openFDA food enforcement)
Reported Apr 6, 2016
Knee Shield (Patella Cup) Product Usage: Knee Shield patella cup is an accessory used with the knee braces to provide…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Ossur H / F
13 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 6, 2016
Thai Fusion Outpost, net weight 5.1 oz. UPC 0 99853 34255 9. Thai Fusion Bulk bag, packaged in a ziploc plastic bag,…
High riskUsing this product could cause serious injury, illness or death — stop using it now.Paradise Farm Organics Inc.
FDA (openFDA food enforcement)
Reported Apr 6, 2016
Helios HL3T and HLT Track Mounted Dental Lights Product Usage: The product is intended for use by dental professionals…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pelton & Crane / Marus / DCI Equipment / KaVo
FDA (openFDA device enforcement)
Reported Apr 6, 2016
The S.C.O.R.E.S. Unit (self contained operating room equipment sterilization unit)
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Pmbs, LLC
FDA (openFDA device enforcement)
Reported Apr 6, 2016
The E.CAM gamma camera system Product Usage: The E.CAM gamma camera system is a SPECT system and measures the…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Apr 6, 2016
Cios Alpha, mobile X-ray system
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
15 more products in this recall
FDA (openFDA device enforcement)
Reported Apr 6, 2016
Synthes Interlocking Bolt, 151 mm (General and Plastics Surgery Devices) Guide, Surgical Instrument
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Synthes (USA) Products LLC
FDA (openFDA device enforcement)
Reported Mar 30, 2016
Arthrex IBalance TKA Tibial Tray Size 2 - Catalog # AR-503-TTTC, Size 3 - Catalog # AR-503-TTTD, Size 4 -Catalog #…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arthrex, Inc.
FDA (openFDA device enforcement)
Reported Mar 30, 2016
Alaris PC Unit, Infusion Pump Model 8000, Part No. TC10005092
Moderate riskThis product could cause temporary or reversible health problems — stop using it.CareFusion 303, Inc.
FDA (openFDA device enforcement)
Reported Mar 30, 2016
syngo X Workplace is a medical workstation for real-time viewing, image manipulation, 3D-visualization, communication,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Mar 30, 2016
Irrigation Clip 30; Intended to position and hold irrigation tubing during surgical procedures.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.The Anspach Effort, Inc.
FDA (openFDA device enforcement)
Reported Mar 30, 2016
Universal Clamp¿ System (IFU reference: SNA027-N-90001). Provides the stability required for solid bone fusion and…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Zimmer Spine, Inc.
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 23, 2016
CORDIS AVANTI + CATHETER SHEATH INTRODUCER SYSTEM The product includes a Catheter Sheath Introducer (CSI) and a vessel…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Cordis Corporation
FDA (openFDA device enforcement)
Reported Mar 23, 2016
Intra operative MRI Systems: Neuro II-SE , Neuro III-SV, iMRI 1.5T A, and iMRI 3T S. Indicated for use as a magnetic…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Deerfield Imaging
FDA (openFDA device enforcement)
Reported Mar 23, 2016
McKesson Horizon Medical Imaging (HMI) products versions 4.6.1 to including 11.9 and McKesson Radiology (MR) products…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Mckesson Medical Immaging
FDA (openFDA device enforcement)
Reported Mar 23, 2016
Accu-Chek Inform II Base Unit as a part of the Accu-Chek Inform II Blood Glucose Monitoring System Accu-Chek inform II…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Roche Diagnostics Operations, Inc.
FDA (openFDA device enforcement)
Reported Mar 23, 2016
Sekure Chemistry Sekisui Diagnostics Acetaminophen L3K Assay, In-vitro Diagnostic Catalog Number: 506-10: R1: 1 x 10ml,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Sekisui Diagnostics P.E.I. Inc.
FDA (openFDA device enforcement)
Reported Mar 23, 2016
Siemens Syngo Dynamics-a Picture Archiving and Communication System (PACS) Model Numbers: 10091805, 10091807, 10091637,…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Siemens Medical Solutions USA, Inc.
FDA (openFDA device enforcement)
Reported Mar 23, 2016
Prime Series Stretchers (Fifth Wheel, Big Wheel and Zoom) Powered stretcher
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Stryker Medical Division
1 more product in this recall
FDA (openFDA device enforcement)
Reported Mar 16, 2016
Super Arrow-Flex Percutaneous Sheath Introducer Sets REF CL-07035 or CL-07635 or CL-07735 or CL-07835 Super Arrow-Flex…
Moderate riskThis product could cause temporary or reversible health problems — stop using it.Arrow International Inc.
FDA (openFDA device 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.