Product Recalls in Colorado
Product recalls affecting Colorado — including food, drugs, consumer products, medical devices, and vehicles distributed to Colorado. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,045 recalls have been distributed to Colorado in the last 12 months.
Showing 23301–23320 of 51,434 recalls
Recalled Item: VITROS 250 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: Potential negative drift in Creatine Kinase (CK) results when used on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill Recalled by Zimmer GmbH Due to An investigation identified that the...
The Issue: An investigation identified that the products were possibly manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drill Sys2.7 Recalled by Zimmer GmbH Due to An investigation identified that...
The Issue: An investigation identified that the products were possibly manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 250AT Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: Potential negative drift in Creatine Kinase (CK) results when used on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 250 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: Potential negative drift in Creatine Kinase (CK) results when used on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity i Processing Module Recalled by Abbott Gmbh & Co. KG Due to...
The Issue: Potential loose cable connections on the reagent cooler, which could result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kopi Jantan Tradisional Natural Herbs Coffee Recalled by Brian P. Richardson...
The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found this product to be...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: cobas p 701 post-analytical units Recalled by Roche Diagnostics Corporation...
The Issue: There is a potential for the tray input flap on the post analytical units to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SoundWave Professional Suite Software 3.2 Recalled by Advanced Bionics, LLC...
The Issue: The manufacturer received complaints that customers were attempting to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas p 501 post-analytical units Recalled by Roche Diagnostics Corporation...
The Issue: There is a potential for the tray input flap on the post analytical units to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Autoimmune EIA Anti-Tissue Transglutaminase (tTG) IgA Test Recalled by...
The Issue: An elevated lot-to-lot bias was observed for Autoimmune EIA Anti-Tissue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T BlueStar Machine Software v.2.72-Hemodialysis machine Model Number:...
The Issue: Power Logic Board Fail Message on the 2008T BlueStar Machine with software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adapter for handpiece Recalled by Thommen Medical AG Due to Dental adaptor...
The Issue: Dental adaptor does not conform to specifications. The dental coupling of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Veritor System Reader -In Vitro Diagnostic for use with Recalled by...
The Issue: Background calibration has the potential to cause false positive or false...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Veritor Plus Analyzer- In-Vitro Diagnostic intended to use with Recalled...
The Issue: Background calibration has the potential to cause false positive or false...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elekta Unity systems Product Usage: Elekta Unity using Magnetic Resonance...
The Issue: There is no warning in the Elekta Unity manual for the administration of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Telmisartan and Amlodipine Tablets 80 mg/5 mg Recalled by AVKARE Inc. Due to...
The Issue: Failed Impurities/Degradation Specifications; 18 month long term stability...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hunts Tomato Paste No Salt Added 6 ounce cans Recalled by ConAgra Foods,...
The Issue: Mold. This situation is due to potential damage to the cans.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Papaverine 30 mg/mL Injection Recalled by Anderson Compounding Pharmacy,...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Prostaglandin 60 mcg/mL Recalled by Anderson Compounding Pharmacy, Inc. DBA...
The Issue: Lack of sterility assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.