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. 2,538 recalls have been distributed to Colorado in the last 12 months.
Showing 21841–21860 of 28,964 recalls
Recalled Item: Flexible Drill Recalled by Aesculap, Inc. Due to The flexible shaft of the...
The Issue: The flexible shaft of the instruments may break during orthopedic spinal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reagent Management System (RMS) Dimension RxL Max w/o HM Product Recalled by...
The Issue: Siemens has identified RMS compressors that are missing the safety cover on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reagent Management System (RMS) Dimension EXL with LM STM Product Recalled...
The Issue: Siemens has identified RMS compressors that are missing the safety cover on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tray Set containing multiple instruments and may contain the flexible bone...
The Issue: The flexible shaft of the instruments may break during orthopedic spinal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arctic Sun Temperature Management System Recalled by C.R. Bard, Inc. Due to...
The Issue: The product may contain electronic components that lead to a premature...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic InSync III Recalled by Medtronic Inc. Due to Medtronic has...
The Issue: Medtronic has confirmed an issue with InSync III CRT-pacemaker devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Remote Patient Monitoring System Recalled by Vidco, Inc. Due to Testing at...
The Issue: Testing at customer site showed unit Remote Patient Monitoring System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxoid Gentamicin Antimicrobial Susceptibility Testing Disc (CN10) Recalled...
The Issue: Antibiotic concentration may be insufficient which may result in incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Unolok Blunt Fill Needle 18G x 1.5" Red Recalled by Myco Medical Supplies...
The Issue: Particulates: Complaints of rubber coring from the closure of injection vials.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Destination Renal Guiding Sheath Intended for the introduction of...
The Issue: Based on internal investigation and testing that revealed the distal end of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RT Elements are applications for radiation treatment planning for use...
The Issue: Large objects with fine resolution are potentially displayed cropped when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RT Elements are applications for radiation treatment planning for use...
The Issue: Large objects with fine resolution are potentially displayed cropped when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Pump SmartSite Infusion Set Recalled by CareFusion 303, Inc. Due to...
The Issue: CareFusion is recalling the Alaris Pump Module SmartSite Infusion Set...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Copper NiTi Preformed Archwires Recalled by Ormco/Sybronendo Due to Ormco...
The Issue: Ormco Corporation is recalling Copper NiTi Preformed Archwires because the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thin-Flex Venous Cannula Recalled by Edwards Lifesciences, LLC Due to...
The Issue: Edwards Lifesciences initiated a field action for the Thin-Flex Venous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...
The Issue: Software anomaly may allow VITROS Systems to sample and process assays while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD10 Recalled by Philips Electronics North America Corporation...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTEGRIS V3000 Recalled by Philips Electronics North America Corporation Due...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD10/10 Recalled by Philips Electronics North America...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTEGRIS CV Recalled by Philips Electronics North America Corporation Due to...
The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.