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. 2,519 recalls have been distributed to Minnesota in the last 12 months.
Showing 19061–19080 of 29,186 recalls
Recalled Item: LeMaitre Vascular Reddick Scoop Tip Cholangiogram Catheter (eIFU) REF#...
The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre Vascular Reddick Cholangiogram Stiffer Catheter with introducer...
The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre Vascular Reddick Cholangiogram Stiffer Catheter (eIFU) REF#...
The Issue: The Contains Latex symbol was not printed onto the box label or the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Table Patient Step on RFX/SFX Recalled by GE Healthcare, LLC Due to Reported...
The Issue: Reported incidents of a patient step detaching from the table. A fall from a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare HVAD System Controller The HeartWare Ventricular Assist System...
The Issue: Product recall of all HVAD Controllers currently on the market and to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee Recalled by Siemens Medical Solutions USA, Inc Due to Failures can...
The Issue: Failures can result due to a component defect on Artis zee systems with an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elcam Minimal Residual Volume Luer-activated Swabable-stockcock (MRVLS) 4w...
The Issue: The stopcock was found to have punctures.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew Dyonics Saw Blade Recalled by Smith & Nephew, Inc. Due to The...
The Issue: The single use devices are provided sterile and do not have an expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew Dyonics Saw Blade Recalled by Smith & Nephew, Inc. Due to The...
The Issue: The single use devices are provided sterile and do not have an expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew Dyonics Saw Blade Recalled by Smith & Nephew, Inc. Due to The...
The Issue: The single use devices are provided sterile and do not have an expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur XPT System Software Versions V1.0.1 Recalled by Siemens...
The Issue: Multiple software issues, which may affect the operation and workflow of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew Dyonics Saw Blade Recalled by Smith & Nephew, Inc. Due to The...
The Issue: The single use devices are provided sterile and do not have an expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew Dyonics Saw Blade Recalled by Smith & Nephew, Inc. Due to The...
The Issue: The single use devices are provided sterile and do not have an expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew Dyonics Saw Blade Recalled by Smith & Nephew, Inc. Due to The...
The Issue: The single use devices are provided sterile and do not have an expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Angio WorkStation (XIDF-AWS801) used in conjunction with your Infinix System...
The Issue: It was found that during a procedure the Peak Skin Dose (PSD) value...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Check-Flo Hemostasis Assembly Recalled by Cook Inc. Due to Devices using a...
The Issue: Devices using a specific hemostatic valve design, to as a blue valve or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Check-Flo Performer Introducer Recalled by Cook Inc. Due to Devices using a...
The Issue: Devices using a specific hemostatic valve design, to as a blue valve or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexor Radial Access Set Recalled by Cook Inc. Due to Devices using a...
The Issue: Devices using a specific hemostatic valve design, to as a blue valve or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Micropuncture Check-Flo Performer Introducer Set Recalled by Cook Inc. Due...
The Issue: Devices using a specific hemostatic valve design, to as a blue valve or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Check-Flo Performer Introducer Set Recalled by Cook Inc. Due to Devices...
The Issue: Devices using a specific hemostatic valve design, to as a blue valve or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.