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. 2,489 recalls have been distributed to Minnesota in the last 12 months.
Showing 24121–24140 of 29,186 recalls
Recalled Item: Accusorb MRI MAC7006 Part Number: MRI-06 MRI-Large Torso Wrap Product...
The Issue: When not used correctly, Accusorb MRI products may overheat and lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accusorb MRI MAC7002 Part Number: MRI-02 MRI-Arm Sleeve Various Sizes...
The Issue: When not used correctly, Accusorb MRI products may overheat and lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INFINITI Ultrasound Pack. Catalog Numbers: 8065751716 Recalled by Alcon...
The Issue: The recalling firm received complaints related to leakage from the tubing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accusorb MRI MAC7007 Part Number: MRI-07 MRI-Breast Shield Product Usage:...
The Issue: When not used correctly, Accusorb MRI products may overheat and lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accusorb MRI MAC7030 Product Usage: Radio frequency shielding blankets and...
The Issue: When not used correctly, Accusorb MRI products may overheat and lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accusorb MRI MAC7009 Part Number: MRI-09 MRI- Leg Wrap Blanket Recalled by...
The Issue: When not used correctly, Accusorb MRI products may overheat and lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accusorb MRI MAC7001 Part Number: MRI-01 MRI-Large Blanket Various Sizes...
The Issue: When not used correctly, Accusorb MRI products may overheat and lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accusorb MRI MAC7003 Part Number: MRI-03 U (Upper) and MRI-03 Recalled by...
The Issue: When not used correctly, Accusorb MRI products may overheat and lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accusorb MRI MAC7010 Product Usage: Radio frequency shielding blankets and...
The Issue: When not used correctly, Accusorb MRI products may overheat and lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accusorb MRI MAC7005 Part Number: MRI-05 Leg Wrap Product Usage: Recalled by...
The Issue: When not used correctly, Accusorb MRI products may overheat and lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FullFire Diffusing Tip Laser Probe Recalled by Monteris Medical Corp Due to...
The Issue: Monteris Medical received a complaint of a separation of the distal sapphire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Avalon Monitors with software revision J.30.58: Model Product FM20...
The Issue: Philips Intellivue and Avalon Fetal Monitors in time-synchronized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SideFire Directional Laser Probe Recalled by Monteris Medical Corp Due to...
The Issue: Monteris Medical received a complaint of a separation of the distal sapphire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips IntelliVue Monitors with software revisions J.21.03 Recalled by...
The Issue: Philips Intellivue and Avalon Fetal Monitors in time-synchronized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natural Knee II Revision Femoral Stem Recalled by Zimmer, Inc. Due to Failed...
The Issue: Failed to meet established requirements for sterile barrier integrity due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Puritan Bennett 980 Ventilator Recalled by Nellcor Puritan Bennett...
The Issue: Covidien is recalling certain Puritan Bennett 980 Ventilator Systems due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tapered Screw-Vent Implant Recalled by Zimmer Dental Inc Due to Zimmer...
The Issue: Zimmer Dental is recalling Tapered Screw-Vent Implants because the incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Puritan Bennett 980 Ventilator Recalled by Nellcor Puritan Bennett...
The Issue: A software issue may lead to ventilator inoperative situations.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Continuum Acetabular System Trabecular Metal Shell with Multi Holes Recalled...
The Issue: The affected products are missing polar boss threads.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: APTUS Ulna Shortening 2.5 Product Usage: APTUS Ulna Shortening 2.5 Recalled...
The Issue: A recall of the APTUS Ulna Shortening 2.5 instrument was initiated due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.