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. 2,509 recalls have been distributed to Colorado in the last 12 months.
Showing 25681–25700 of 28,964 recalls
Recalled Item: Stryker brand COMPLIANT 4MM X 30MM Recalled by Stryker Neurovascular Due to...
The Issue: Products were shipped labeled with "use by" dates that exceed currently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker brand COMPLIANT 5MM X 30MM Recalled by Stryker Neurovascular Due to...
The Issue: Products were shipped labeled with "use by" dates that exceed currently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker brand EXCELSIOR SL-10 PRE-SHAPED S 15OCM Recalled by Stryker...
The Issue: Products were shipped labeled with "use by" dates that exceed currently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker brand GDC VORTX 2MM X 3MM Recalled by Stryker Neurovascular Due to...
The Issue: Products were shipped labeled with "use by" dates that exceed currently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker brand COMPLIANT 4MM X 20MM Recalled by Stryker Neurovascular Due to...
The Issue: Products were shipped labeled with "use by" dates that exceed currently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker brand COMPLIANT 5MM X 15MM Recalled by Stryker Neurovascular Due to...
The Issue: Products were shipped labeled with "use by" dates that exceed currently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker brand EXCELSIOR SL-10 PRE-SHAPED 45 150CM Recalled by Stryker...
The Issue: Products were shipped labeled with "use by" dates that exceed currently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acetabular Pressurizer Recalled by Stryker Instruments Div. of Stryker...
The Issue: On March 14, 2013 a Work Order was opened for 120 units (20 boxes) of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abbott Acclaim Infusion Pump Designed to deliver parenteral infusions...
The Issue: Hospira has received customer reports of broken door assemblies on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hospira Acclaim Encore Infusion Pump Designed to deliver parenteral...
The Issue: Broken door assemblies on the Hospira/Abbott Acclaim Encore infusion pumps....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen¿ Complete Knee Solutions Stemmed Tibial Component Precoat NexGen...
The Issue: Two complaints were received in which it was reported that the stem would...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vasoview Hemopro Endoscopic Vessel Harvesting System Maquet Cardiovascular...
The Issue: Maquet has received an increase in the number of complaints for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medcare Products Max-500 Stand Recalled by Ergosafe Products LLC DBA Prism...
The Issue: The lift might fail with the labeled 500-lb. load rating.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Easy Diagnost Eleva Universal Fluoroscopic applications Recalled by Philips...
The Issue: The delivered application software was an outdated version to the model of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medcare Products Max-500 Stand-N-Weigh Recalled by Ergosafe Products LLC DBA...
The Issue: The lift might fail with the labeled 500-lb. load rating.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAS Urinalysis Control Level 1 Recalled by Thermofisher Scientive Due to Via...
The Issue: Via one (1) consumer complaint and in-house testing has confirmed that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azure Anterior Cervical Plate System Recalled by Orthofix, Inc Due to There...
The Issue: There is a possibility that the locking mechanism of the Azure Anterior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dura Guard Recalled by Synovis Surgical Innovations, Inc. Due to Synovis, a...
The Issue: Synovis, a subsidiary of Baxter International Inc., is recalling certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vascu Guard Recalled by Synovis Surgical Innovations, Inc. Due to Synovis, a...
The Issue: Synovis, a subsidiary of Baxter International Inc., is recalling certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1) Nephros SafeShower FH - 15 filters per box Recalled by Nephros Inc Due to...
The Issue: Promotional materials for non-medical water filtration products were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.