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. 1,119 recalls have been distributed to Colorado in the last 12 months.
Showing 14401–14420 of 28,964 recalls
Recalled Item: Drill for 2.7mm screw Recalled by Zimmer GmbH Due to An investigation...
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 for 2.7mm screw Recalled by Zimmer GmbH Due to An investigation...
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 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 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 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 for 2.7mm screw Recalled by Zimmer GmbH Due to An investigation...
The Issue: An investigation identified that the products were possibly manufactured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MaxiCan 4.5 countersink Recalled by Zimmer GmbH Due to An investigation...
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 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: V-TEK" 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 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: V-TEK" 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: V-TEK" 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 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 for 2.7mm screw Recalled by Zimmer GmbH Due to An investigation...
The Issue: An investigation identified that the products were possibly manufactured...
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: 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: 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: 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: 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: 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.