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. 2,723 recalls have been distributed to Colorado in the last 12 months.
Showing 2661–2680 of 51,434 recalls
Recalled Item: Levothyroxine Sodium Tablets Recalled by ACCORD HEALTHCARE, INC. Due to...
The Issue: Subpotent
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothyroxine Sodium Tablets Recalled by ACCORD HEALTHCARE, INC. Due to...
The Issue: Subpotent
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levothyroxine Sodium Tablets Recalled by ACCORD HEALTHCARE, INC. Due to...
The Issue: Subpotent
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: clomiPRAMINE hydrochloride Capsules USP Recalled by Lupin Pharmaceuticals...
The Issue: Failed Impurities/Degradation Specifications: an out of specification result...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Testosterone Cypionate Injection Recalled by Eugia US LLC Due to cGMP:...
The Issue: cGMP: complaints of crystals not redissolving into solution after warming...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 3M Ranger Blood/Fluid Warming High Flow Set Catalog Numbers 24355 Recalled...
The Issue: Field action to clarify the flow rates and inlet fluid temperatures, along...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: AirLife Product Name: AirLife Infant Heated Wire Circuit...
The Issue: Adapters may disconnect during setup or while in use, potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CMS8000 Patient Monitor Recalled by Contec Medical Systems Co., Ltd. Due to...
The Issue: Patient monitor has nine identified cybersecurity vulnerabilities.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: AirLife Product Name: AirLife Infant Heated Wire Circuit...
The Issue: Adapters may disconnect during setup or while in use, potentially...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD-Solis HPCA Ambulatory Infusion Pump Recalled by Smiths Medical ASD,...
The Issue: Affected pumps may trigger an erroneous (false) Upstream Occlusion Alarm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD-Solis VIP Ambulatory Infusion Pump Recalled by Smiths Medical ASD, Inc....
The Issue: Affected pumps may trigger an erroneous (false) Upstream Occlusion Alarm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD Solis VIP Ambulatory Infusion Pump Models: 1) PUMP KIT Recalled by...
The Issue: There is a potential for thermal damage in CADD-Solis and CADD- Solis VIP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD-Solis Infusion Pump Models: 1) PUMP KIT Recalled by Smiths Medical ASD,...
The Issue: There is a potential for thermal damage in CADD-Solis and CADD- Solis VIP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CADD Solis HSPCA Pump Recalled by Smiths Medical ASD, Inc. Due to Pumps may...
The Issue: Pumps may experience Wireless Connection Modules intermittent connection...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blueprint Software Recalled by Tornier S.A.S. Due to A software bug in...
The Issue: A software bug in Blueprint version 4.2.1 prevents users from accessing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centurion Sterile Weitlaner Retractor 3 x 4 Prong Recalled by MEDLINE...
The Issue: Three is the potential for the retractors to puncture through the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FoundationOne Companion Diagnostic (F1CDx) Recalled by Foundation Medicine,...
The Issue: Four (4) total reports were sent to customers with clinically relevant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centurion Sterile Weitlaner Retractor Recalled by MEDLINE INDUSTRIES, LP -...
The Issue: Three is the potential for the retractors to puncture through the sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: REMISOL Advance UDI-DI code: 13700962601874 All Software Versions: B92487...
The Issue: Due to a software issue, the software may incorrectly process the date of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artix MT Thrombectomy Device Recalled by Inari Medical - Oak Canyon Due to...
The Issue: Thrombectomy device specifies vessel range of 2.5-6 mm on the pouch, carton,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.