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. 2,563 recalls have been distributed to Minnesota in the last 12 months.
Showing 17201–17220 of 29,186 recalls
Recalled Item: Unifine Pentips 5mm x 31G pen needles Recalled by Owen Mumford USA, Inc. Due...
The Issue: Device may potentially be compromised by water in end user packaging....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Innova Self-Expanding Stent System Recalled by Boston Scientific Corporation...
The Issue: Stent possibly unable to be fully released from the delivery system.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Innova Self-Expanding Stent System Recalled by Boston Scientific Corporation...
The Issue: Stent possibly unable to be fully released from the delivery system.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alden Classic 55 Toric Daily Wear Soft contact Recalled by Alden Optical Due...
The Issue: Contact lenses lack sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alden HP49 Sphere Daily Wear Soft contact Recalled by Alden Optical Due to...
The Issue: Contact lenses lack sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Handicare C Series Patient Lift Product Usage: A device used Recalled by...
The Issue: Premature strap wear and breakage at maximum weight conditions (625 lbs.).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovaKone Daily Wear Soft contact Recalled by Alden Optical Due to Contact...
The Issue: Contact lenses lack sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alden HP54 Toric Daily Wear Soft contact Recalled by Alden Optical Due to...
The Issue: Contact lenses lack sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NovaKone Toric Daily Wear Soft contact Recalled by Alden Optical Due to...
The Issue: Contact lenses lack sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alden HP59 Sphere Daily Wear Soft contact Recalled by Alden Optical Due to...
The Issue: Contact lenses lack sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bvi Beaver Xstar Safety Crescent Recalled by Beaver-Visitec International...
The Issue: The protective shield was retracted, and the blade was exposed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bvi Beaver Safety Sideport Knife: (a) 1.0mm Recalled by Beaver-Visitec...
The Issue: The protective shield was retracted, and the blade was exposed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Handicare P600 Series Patient Lift Product Usage: A device used Recalled by...
The Issue: Premature strap wear and breakage at maximum weight conditions (625 lbs.).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bvi Beaver EdgeAhead Safety Knife Recalled by Beaver-Visitec International...
The Issue: The protective shield was retracted, and the blade was exposed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Everflex Self-Expanding Peripheral Stent with Entrust Delivery System...
The Issue: Stent length on the label may not match the length of the stent itself.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volcano Imaging System s5i Recalled by Volcano Corporation Due to On certain...
The Issue: On certain Impacted Systems, an unexpected Microsoft Windows Security dialog...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alden HP54 Sphere Daily Wear Soft contact Recalled by Alden Optical Due to...
The Issue: Contact lenses lack sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alden HP49 Toric Daily Wear Soft contact Recalled by Alden Optical Due to...
The Issue: Contact lenses lack sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ASTERA Multifocal Toric Daily Wear Soft contact Recalled by Alden Optical...
The Issue: Contact lenses lack sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alden HP59 Toric Daily Wear Soft contact Recalled by Alden Optical Due to...
The Issue: Contact lenses lack sterility assurance.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.