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. 2,422 recalls have been distributed to Minnesota in the last 12 months.
Showing 41141–41160 of 52,120 recalls
Recalled Item: Siemens Healthcare Caps for capillary 140/175 uL Recalled by Siemens...
The Issue: Capillary Caps for RAPIDLyte Multicap and Multicap-S Blood Collection...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Healthcare Caps for capillary 50/60 uL Recalled by Siemens...
The Issue: Capillary Caps for RAPIDLyte Multicap and Multicap-S Blood Collection...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Healthcare Caps for capillary 100 uL Recalled by Siemens Healthcare...
The Issue: Capillary Caps for RAPIDLyte Multicap and Multicap-S Blood Collection...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Restoris Partial Knee Application (PKA) RIO (TGS 2.0). For use Recalled by...
The Issue: When using the MAKOplasty partial knee Arthroplasty application, the burr...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FORUM Archive and Viewer Recalled by Carl Zeiss Meditec AG Due to Software...
The Issue: Software defect in the FORUM Viewer versions 3.1 and 3.2 which may lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ketorolac Tromethamine Ophthalmic Solution Recalled by Sun Pharma Global Fze...
The Issue: Presence of Particulate Matter: lot is not meeting the specification limit...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levetiracetam Recalled by Sun Pharma Global Fze Due to Failed Dissolution...
The Issue: Failed Dissolution Specifications: 6 month time point.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Merge Hemo Recalled by Merge Healthcare, Inc. Due to A system freeze-up of...
The Issue: A system freeze-up of the Merge Hemo system, that included the PHASEIN End...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens LANTIS Oncology Information System Servers Recalled by Siemens...
The Issue: There is a potential safety risk when using LANTIS server software with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DynaLOC Breast Interventional Planning Software Versions 3.1 and 3.2...
The Issue: A device malfunction may cause the biopsy needle to fail to reach the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aquarius iNtuition Client Viewer. Findings Workflow module Recalled by...
The Issue: Software anomaly related to RECIST1.1 target lesion evaluation criteria in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemodialysis Catheters and PICCs: Product identification: MCDLTSL24P (SF X...
The Issue: Drug products contained within the kits may have been rendered ineffective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Avastin (Bevacizumab) 2 mg/0.08 mL syringe Recalled by Pacifico National,...
The Issue: Non-Sterility: Product tested positive for bacterial contamination.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Avastin (Bevacizumab) 1.25 mg/0.05 mL syringe Recalled by Pacifico National,...
The Issue: Non-Sterility: Product tested positive for bacterial contamination.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by Hospira Inc. Due to Presence of...
The Issue: Presence of Particulate Matter; Hospira has identified the particulate as a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ADVIA Chemistry Systems Drug Calibrator I Recalled by Siemens Healthcare...
The Issue: Incorrect calibrator lot values were assigned for ADVIA Chemistry Systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Chopped Twix Recalled by Tarrier Foods Corp Due to Undeclared Allergens
The Issue: The firm's Chopped Twix candy may contain undeclared allergens: peanuts and...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Streit's Kids Dark CHOCOLATE Coins Recalled by Aron Streit Inc. Due to...
The Issue: State of New York Department of Agriculture and Markets tested revealed...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: KimVent Closed Suction System for Adults Recalled by Halyard Health Due to...
The Issue: Defect: A hole or crack was found which may cause air to leak.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KimVent Closed Suction System for Adults Recalled by Halyard Health Due to...
The Issue: Defect: A hole or crack was found which may cause air to leak.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.