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 21141–21160 of 52,120 recalls
Recalled Item: Torcon NB Advantage Catheters - Product Usage: Intended for use Recalled by...
The Issue: The potential compromise of the sterility of products from an undersealed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Torcon NB Advantage Catheters - Product Usage: Intended for use Recalled by...
The Issue: The potential compromise of the sterility of products from an undersealed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Torcon NB Advantage Catheters - Product Usage: Intended for use Recalled by...
The Issue: The potential compromise of the sterility of products from an undersealed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CS5/5+ Fastpacks Recalled by Haemonetics Corporation Due to Potential to...
The Issue: Potential to develop leaks at the inner core of Cell Saver¿ 5/5+ and Cell...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System Recalled by Integra...
The Issue: The 36 kHz Sterilization Tray (C7136 Rev C / 72904491 Rev A) system does not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System Recalled by Integra...
The Issue: The 36 kHz Sterilization Tray (C7136 Rev C / 72904491 Rev A) system does not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DxM 1040 MicroScan WalkAway Instrument Recalled by Beckman Coulter Inc. Due...
The Issue: WalkAway Instruments may have been assembled with the incorrect AC power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan WalkAway-96 plus Reconditioned Instrument Recalled by Beckman...
The Issue: WalkAway Instruments may have been assembled with the incorrect AC power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan WalkAway-40 plus Reconditioned Instrument Recalled by Beckman...
The Issue: WalkAway Instruments may have been assembled with the incorrect AC power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan WalkAway-96 plus Instrument Recalled by Beckman Coulter Inc. Due...
The Issue: WalkAway Instruments may have been assembled with the incorrect AC power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DxM 1096 MicroScan WalkAway Instrument Recalled by Beckman Coulter Inc. Due...
The Issue: WalkAway Instruments may have been assembled with the incorrect AC power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan WalkAway-40 plus Instrument Recalled by Beckman Coulter Inc. Due...
The Issue: WalkAway Instruments may have been assembled with the incorrect AC power...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PF-Succinylcholine Chloride Injection Recalled by Nephron Pharmaceuticals...
The Issue: Incorrect labeling: Incorrect or missing lot and/or exp date
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Prasugrel Tablets 5 mg Recalled by Mylan Pharmaceuticals Inc. Due to Failed...
The Issue: Failed Dissolution Specification: Low out of specification dissolution results.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Aequalis Ascend Flex Humeral Stem: Part Number UDI DWF601A 3700386944475...
The Issue: During shipping, it is possible for the Aequalis Ascend Flex humeral stem to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BRASSELER KM166-310-35 Twist Drill Quick Connect Diameter 3.5 mm Recalled by...
The Issue: One lot of 3.5 mm twist drills were incorrectly laser etched as 2.5 mm the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bimatoprost Ophthalmic Solution 0.03% Recalled by Sandoz Inc Due to...
The Issue: Labeling: Incorrect or missing package insert.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Gatifloxacin Ophthalmic Solution 0.5% Recalled by Sandoz Inc Due to...
The Issue: Labeling: Incorrect or missing package insert.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Neomycin and Polymyxin B Sulfates and Dexamethasone Ophthalmic Suspension...
The Issue: Labeling: Incorrect or missing package insert.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HeartStart XL+ Defibrillator/Monitor Recalled by Philips North America, LLC...
The Issue: The rotary therapy selector switch may fail, resulting in unexpected device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.