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. 2,634 recalls have been distributed to Colorado in the last 12 months.
Showing 12661–12680 of 51,434 recalls
Recalled Item: BD Connecta Stopcock with OFF Directed Tap Without Extension Tube Recalled...
The Issue: May have the potential for leakage at the housing component of the stopcock,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: medroxyPROGESTERone Acetate Injectable Suspension Recalled by SUN...
The Issue: Lack of assurance of sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: medroxyPROGESTERone Acetate Injectable Suspension Recalled by SUN...
The Issue: Lack of assurance of sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: medroxyPROGESTERone Acetate Injectable Suspension Recalled by SUN...
The Issue: Lack of assurance of sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: medroxyPROGESTERone Acetate Injectable Suspension Recalled by SUN...
The Issue: Lack of assurance of sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: medroxyPROGESTERone Acetate Injectable Suspension Recalled by SUN...
The Issue: Lack of assurance of sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) Delivers 10 mg over 9 hours...
The Issue: Defective Delivery System: customer complaints exceeded respective action...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VOLISTA StandOP Surgical Light Recalled by Getinge Usa Sales Inc Due to...
The Issue: Paint particles may detach and fall in the operating field. In the worst...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KWIK-STIK" plus: Clostridium perfringens Recalled by Microbiologics Inc Due...
The Issue: Labeling error.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Equate Tartar Control Plus (Eucalyptol 0.092% Recalled by Vi-Jon, LLC Due to...
The Issue: Superpotent Drug: product complaint for milky blue appearance and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Valencian Almonds FS Skinless Recalled by Power Selles Imports dba Culinary...
The Issue: Potential contamination with peanut while label does not declare peanut.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Arrow Three-Lumen CVC Recalled by ARROW INTERNATIONAL Inc. Due to Gravity...
The Issue: Gravity flow rates on the affected product lidstock are incorrect.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartWare Battery Recalled by Medtronic Inc Due to Batteries for the HVAD...
The Issue: Batteries for the HVAD system have a weld defect affecting internal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nester Embolization Microcoil RPN GPN MWCE-18-5-2-NESTER G52733...
The Issue: The loading cartridges included with these devices may contain a small,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tornado Embolization Microcoil Recalled by Cook Incorporated Due to The...
The Issue: The loading cartridges included with these devices may contain a small,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hilal Embolization Microcoil Recalled by Cook Incorporated Due to The...
The Issue: The loading cartridges included with these devices may contain a small,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DJO EMPOWR 3D Knee (Right) 10mm Tibial Insert Recalled by Encore Medical, LP...
The Issue: A right, size 8, knee tibial insert package may include a mispackaged, left...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optiflux 200NRe Dialyzer Finished Assy. Recalled by Fresenius Medical Care...
The Issue: Dialyzers were distributed after being exposed to cold temperatures which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROFEMUR PLASMA Z CLASSIC STEM SIZE 7 STANDARD SHORT NECK Recalled by...
The Issue: One manufacturing lot is missing the plasma-spray coating in the proximal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nitrofurantoin Capsules Recalled by American Health Packaging Due to Failed...
The Issue: Failed Dissolution Specifications: Nitrofurantoin Capsules recalled due to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.