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. 2,666 recalls have been distributed to Minnesota in the last 12 months.
Showing 5581–5600 of 29,186 recalls
Recalled Item: Mobile airway scope-diagnosis and observation to access airway anatomy...
The Issue: Channel air drying process was not validated, and that a small percentage of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hysteroscope-For endoscopic diagnosis within the uterus Model Number:...
The Issue: Channel air drying process was not validated, and that a small percentage of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uretero-reno fiberscope-For endoscopic diagnosis and treatment within the...
The Issue: Channel air drying process was not validated, and that a small percentage of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arial Water Resistant Pendant with Long Wristband Recalled by Securitas...
The Issue: Premature battery depletion presents a risk that alarms will not be received...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RSP Humeral Socket Insert Size 36mm Semi-Constrained +4 mm Recalled by...
The Issue: Two different humeral socket Insert devices were swapped during packaging,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arial Water Resistant Pendant with Wristband Recalled by Securitas...
The Issue: Premature battery depletion presents a risk that alarms will not be received...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arial Water Resistant Pendant with Neck Lanyard Recalled by Securitas...
The Issue: Premature battery depletion presents a risk that alarms will not be received...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RSP Humeral Small Socket Insert Size 32 mm Semi-Constrained +4 Recalled by...
The Issue: Two different humeral socket Insert devices were swapped during packaging,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SPRYSTEP VECTOR KAFO Recalled by Townsend Design Due to Due to potential air...
The Issue: Due to potential air pockets between layers of material, their is the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CUSTOM SPRYSTEP Recalled by Townsend Design Due to Due to potential air...
The Issue: Due to potential air pockets between layers of material, their is the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SPRYSTEP VECTOR Recalled by Townsend Design Due to Due to potential air...
The Issue: Due to potential air pockets between layers of material, their is the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DBX Demineralized Bone Matrix Putty 10cc-Indicated for treatment of...
The Issue: Units are labeled as 10cc; however the units have a fill volume of 1cc...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus High-Flow Insufflation Unit Recalled by Olympus Corporation of the...
The Issue: There have been reports of patients suffering arrhythmias, reported as short...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost 4 Chest/Emergency Recalled by Philips North America Llc Due...
The Issue: Potential for units suspended on the ceiling to fail and fall.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CombiDiagnost R90 Recalled by Philips North America Llc Due to Potential for...
The Issue: Potential for units suspended on the ceiling to fail and fall.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost 4 High Performance Recalled by Philips North America Llc Due...
The Issue: Potential for units suspended on the ceiling to fail and fall.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost C90 Release 3 Recalled by Philips North America Llc Due to...
The Issue: Potential for units suspended on the ceiling to fail and fall.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost C90 Release 3.1 Recalled by Philips North America Llc Due to...
The Issue: Potential for units suspended on the ceiling to fail and fall.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProxiDiagnost N90 Recalled by Philips North America Llc Due to Potential for...
The Issue: Potential for units suspended on the ceiling to fail and fall.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost C90 High Performance Recalled by Philips North America Llc...
The Issue: Potential for units suspended on the ceiling to fail and fall.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.