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. 2,439 recalls have been distributed to Minnesota in the last 12 months.
Showing 36461–36480 of 52,120 recalls
Recalled Item: TF Adaptive Gutta Percha Point Size SM3 50pk Recalled by Ormco/Sybronendo...
The Issue: Ormco Corporation is recalling the TF Adaptive Gutta Percha Point Size...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tudorza Pressair (aclindinium bromide inhalation powder) Recalled by...
The Issue: Defective Delivery System: Some units have actuation counters set to a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Paricalcitol Capsules Recalled by Teva Pharmaceuticals USA Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: Out of specification test...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Irrigation Recalled by Baxter Healthcare Corp. Due to...
The Issue: PRESENCE OF PARTICULATE MATTER: Product complaint for the presence of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Living Tree Community Foods Organic Macadamia Butter Recalled by Living Tree...
The Issue: Recall of macadamia nuts and macadamia butter after notification by...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Living Tree Community Foods Organic Macadamia Nuts Recalled by Living Tree...
The Issue: Recall of macadamia nuts and macadamia butter after notification by...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Allegra X-5 rotor yoke Recalled by Beckman Coulter Inc. Due to A defective...
The Issue: A defective rotor yoke on Allegra X-5 allows improper rotor seating on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance iCT SP Computed Tomography X-ray Systems Recalled by Philips...
The Issue: The firm was notified of a software error in which the system may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity CT Computed Tomography X-ray Systems Recalled by Philips Medical...
The Issue: The firm was notified of a software error in which the system may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance 64:Computed Tomography X-ray Systems Recalled by Philips Medical...
The Issue: The firm was notified of a software error in which the system may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core 128 Computed Tomography X-ray Systems Recalled by Philips...
The Issue: The firm was notified of a software error in which the system may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenuity Core Computed Tomography X-ray Systems Recalled by Philips Medical...
The Issue: The firm was notified of a software error in which the system may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance iCT Computed Tomography X-ray Systems Recalled by Philips Medical...
The Issue: The firm was notified of a software error in which the system may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transport Stretcher Recalled by Stryker Medical Division of Stryker...
The Issue: The hydraulic jack assemblies (PN: 0753-002-101, 0753-002-070, 0753-002-001,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prime Series Stretchers (Fifth Wheel Recalled by Stryker Medical Division of...
The Issue: The hydraulic jack assemblies (PN: 0753-002-101, 0753-002-070, 0753-002-001,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volcano R100 Sterile Equipment Cover Recalled by Volcano Corporation Due to...
The Issue: Volcano Corporation has identified that certain lot numbers of Volcano R-100...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volcano SpinVision Sterile Equip cover II Recalled by Volcano Corporation...
The Issue: Volcano Corporation has identified that certain lot numbers of Volcano R-100...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fentanyl Citrate 1.275 mg/ml/Baclofen 150 mcg/ml/Bupivacaine HCL 20 mg/ml/...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydromorphone HCL 25 mg/ml/Bupivacaine HCL 4 mg/ml Recalled by Hartley...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydromorphone HCL 10 mg/ml Recalled by Hartley Medical Center Pharmacy,...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.