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. 2,693 recalls have been distributed to Minnesota in the last 12 months.
Showing 2521–2540 of 29,186 recalls
Recalled Item: MISHA Knee System Implant Small Recalled by Moximed, Inc. Due to Knee...
The Issue: Knee implant may fracture due to a supplier-related issue with one component...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OsteoSurge 100 Demineralized Bone Matrix Putty with Accell Bone Matrix...
The Issue: Incorrect expiration date listed on the outer box, which does not align with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OsteoCove Putty Recalled by IsoTis OrthoBiologics, Inc. Due to Hydration...
The Issue: Hydration issue resulting in the product being less cohesive and moldable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: HALYARD Product Name: Laparotomy Pack Model/Catalog Number:...
The Issue: Elevated residues of anti-block/slip additive used in manufacturing found...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access Intact PTH assay Recalled by Beckman Coulter, Inc. Due to Beckman...
The Issue: Beckman Coulter has identified that some Access PTH reagent packs from lot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Unitek Transbond Plus Self-Etching Primer (100 unit Recalled by 3M Unitek...
The Issue: Due to an increase of complaints for bracket bond failures and skin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...
The Issue: The probe tips of the hand instruments are being damaged or breaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...
The Issue: The probe tips of the hand instruments are being damaged or breaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...
The Issue: The probe tips of the hand instruments are being damaged or breaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...
The Issue: The probe tips of the hand instruments are being damaged or breaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...
The Issue: The probe tips of the hand instruments are being damaged or breaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...
The Issue: The probe tips of the hand instruments are being damaged or breaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...
The Issue: The probe tips of the hand instruments are being damaged or breaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...
The Issue: The probe tips of the hand instruments are being damaged or breaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...
The Issue: The probe tips of the hand instruments are being damaged or breaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...
The Issue: The probe tips of the hand instruments are being damaged or breaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument...
The Issue: The probe tips of the hand instruments are being damaged or breaking...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AURYON LASER SYSTEM 100-120 VAC. Model Number: EXM001. Product Number:...
The Issue: Potential for procedural delays or interruptions during use of the Auryon...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xhibit Telemetry Receiver Recalled by Spacelabs Healthcare, Inc. Due to...
The Issue: Telemetry receiver systems may experience a Windows proxy Issue causing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Xhibit Telemetry Receiver with Software Recalled by Spacelabs Healthcare,...
The Issue: Telemetry receivers with affected software versions may experience...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.