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. 970 recalls have been distributed to Colorado in the last 12 months.
Showing 43381–43400 of 51,434 recalls
Recalled Item: Synthes Guide Blocks for the 2 Column Plate 6 Hole Recalled by Synthes, Inc....
The Issue: The Guide Blocks for the 2 Column Plate 6 Hole Head (Volar Distal Radius...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fluvastatin Capsules USP Recalled by Teva Pharmaceuticals USA Due to Failed...
The Issue: Failed Tablet/Capsule Specifications: Teva Pharmaceuticals USA, Inc. is...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Coca Cola Vanilla Recalled by The Coca-Cola Company Due to Undeclared Aspartame
The Issue: The product contains undeclared aspartame.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: William & Sonoma Navitas Naturals brand Omega 3 Smoothie Mixer Recalled by...
The Issue: Data obtained from interviews of patients in a multistate outbreak of...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Navitas Naturals Organic Sprouted Chia Powder Recalled by Navitas, LLC., dba...
The Issue: Data obtained from interviews of patients in a multistate outbreak of...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Navitas Naturals Omega Blend Sprouted Smoothie Mix Recalled by Navitas,...
The Issue: Data obtained from interviews of patients in a multistate outbreak of...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Foradil Aerolizer (formoterol fumarate inhalation powder) Recalled by...
The Issue: Failed Stability Specification; out of specification result for particle...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: HydroFinity Hydrophilic guidewire Recalled by Nitinol Devices and...
The Issue: Reports of outer polymer jacket to the core wire being damaged during use on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydroFinity Hydrophilic guidewire Recalled by Nitinol Devices and...
The Issue: Reports of outer polymer jacket to the core wire being damaged during use on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gel-E Donut Recalled by Childrens Medical Ventures Due to The gel-filled...
The Issue: The gel-filled Gel-E Donut and Squishon product line has received a number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydroFinity Hydrophilic guidewire Recalled by Nitinol Devices and...
The Issue: Reports of outer polymer jacket to the core wire being damaged during use on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydroFinity Hydrophilic guidewire Recalled by Nitinol Devices and...
The Issue: Reports of outer polymer jacket to the core wire being damaged during use on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abacus 3.1 Recalled by Baxter Corporation Englewood Due to Baxter...
The Issue: Baxter Corporation is initiating a field correction following an upgrade to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydroFinity Hydrophilic guidewire Recalled by Nitinol Devices and...
The Issue: Reports of outer polymer jacket to the core wire being damaged during use on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydroFinity Hydrophilic guidewire Recalled by Nitinol Devices and...
The Issue: Reports of outer polymer jacket to the core wire being damaged during use on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Linear Accelerators of type ARTISTE Recalled by Siemens Medical...
The Issue: A safety risk exists with automatically sequenced treatment technique using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydroFinity Hydrophilic guidewire Recalled by Nitinol Devices and...
The Issue: Reports of outer polymer jacket to the core wire being damaged during use on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydroFinity Hydrophilic guidewire Recalled by Nitinol Devices and...
The Issue: Reports of outer polymer jacket to the core wire being damaged during use on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydroFinity Hydrophilic guidewire Recalled by Nitinol Devices and...
The Issue: Reports of outer polymer jacket to the core wire being damaged during use on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HydroFinity Hydrophilic guidewire Recalled by Nitinol Devices and...
The Issue: Reports of outer polymer jacket to the core wire being damaged during use on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.