Product Recalls in Minnesota
Product recalls affecting Minnesota — including food, drugs, consumer products, medical devices, and vehicles distributed to Minnesota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,518 recalls have been distributed to Minnesota in the last 12 months.
Showing 19781–19800 of 29,186 recalls
Recalled Item: 2.5 mm Reaming Rod with Ball Tip & Extension/950 mm Recalled by Synthes...
The Issue: The peel pouches for the affected reaming rods and extraction hooks are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.5 mm Reaming Rod W/Ball Tip 650 mm Recalled by Synthes (USA) Products LLC...
The Issue: The peel pouches for the affected reaming rods and extraction hooks are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.5 mm Guide Rod w/Smooth Tip 950 mm Recalled by Synthes (USA) Products LLC...
The Issue: The peel pouches for the affected reaming rods and extraction hooks are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic SynchroMed II Implantable Drug Infusion System. This system...
The Issue: Medtronic is following up to a May 2013 communication regarding the Priming...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Extraction Hook - Sterile for TI Cannulated Nails Recalled by Synthes (USA)...
The Issue: The peel pouches for the affected reaming rods and extraction hooks are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Model 37751 Recharger Product Usage: The Medtronic 37751 Recharger is...
The Issue: Medtronic has identified an increased number of complaints from customers...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4205 Journey Rolling Walker Product Usage: used to assist people in walking...
The Issue: Nova Medical is recalling the Journey Rolling Walker because the screws used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lumex Recalled by GF Health Products, Inc Due to GF Health Products, Inc.,...
The Issue: GF Health Products, Inc., in conjunction with OKIN America, has initiated a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PET Infusion Pump Recalled by Bayer Healthcare Due to The Source...
The Issue: The Source Administration Sets (SAS) used with the Medrad Intego PET...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Devon Light Glove packaged in sterile surgical kits : Recalled by...
The Issue: Added Instructions for Use: After application, inspect the Light Glove for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aptio Automation Modules Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: Possible overheating of power cord plugs used to connect to FlexLab and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The ORCHESTRA PLUS Programmer A portable device Recalled by Sorin Group USA,...
The Issue: Sorin Group USA, Inc. announces a voluntary field action for the ORCHESTRA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thayer MiniSpacer Dual Spray MDI Adapter Counter Incrementing Actuator with...
The Issue: The insert and case label description of the device incorrectly reads...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Restoris RIO Reamer Handle Recalled by Mako Surgical Corporation Due...
The Issue: Failure of the Offset Cup Reamer Handle not engaging its mating components.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The ORCHESTRA Programmer A portable device Recalled by Sorin Group USA, Inc....
The Issue: Sorin Group USA, Inc. announces a voluntary field action for the ORCHESTRA...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FlexLab Automation Modules Recalled by Siemens Healthcare Diagnostics, Inc....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Professional Hospital Supply Recalled by Covidien LLC Due to Added...
The Issue: Added Instructions for Use: After application, inspect the Light Glove for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Devon Light Glove sub-assembly non-sterile For Kit Packers Product...
The Issue: Added Instructions for Use: After application, inspect the Light Glove for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter SIGMA Spectrum INFUSION PUMP with Master Drug Library Recalled by...
The Issue: A correction was issued for the SIGMA Spectrum Infusion Pump with Master...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 4...
The Issue: Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.