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. 2,724 recalls have been distributed to Colorado in the last 12 months.
Showing 1321–1340 of 28,964 recalls
Recalled Item: Brand Name: EMPOWR 3D KNEE TIBIAL INSERT - E-PLUS Product Recalled by Encore...
The Issue: Knee implants contain incorrect labeling (size and/or side incorrect)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: EMPOWR 3D KNEE TIBIAL INSERT - E-PLUS Product Recalled by Encore...
The Issue: Knee implants contain incorrect labeling (size and/or side incorrect)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ambu SPUR II Labeled as the following: 1 SPUR II Adult Resuscitator Recalled...
The Issue: Potential for the manometer port being blocked rendering the manometer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microbore Extension Set with 0.2 Micron Filter. Catalog Number: V6215....
The Issue: Label is incorrect. The product label indicates that the device contains an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vercise Deep Brain Stimulation Systems Surgical Implant Manual Recalled by...
The Issue: Wire break(s) have occurred in rechargeable deep brain stimulation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Medline General Surgery Tray is customized to meet requirements Recalled...
The Issue: Affected kits contain recalled Stryker Color Cuff Sterile Disposable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Burr Hole Cover Kit Recalled by Boston Scientific Neuromodulation...
The Issue: Resistance and difficulties could occur while closing the retaining clip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Trucount Controls Recalled by Becton, Dickinson and Company, BD Bio...
The Issue: Control kits contain incorrect standard deviation (SD) values for the low...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Trucount Controls Recalled by Becton, Dickinson and Company, BD Bio...
The Issue: Control kits contain incorrect standard deviation (SD) values for the low...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Alaris Pump Infusion Sets Recalled by CareFusion 303, Inc. Due to...
The Issue: Infusion pump module used with compatible pump infusion sets may perform...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Alaris Pump Module Model Recalled by CareFusion 303, Inc. Due to Infusion...
The Issue: Infusion pump module used with compatible pump infusion sets may perform...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carotid WALLSTENT Monorail Endoprosthesis Closed Cell Self-Expanding Stent...
The Issue: Certain batches are being removed due to an increase in complaints received...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: epoc BGEM BUN Test Card [25pk]. Material Number: 10736515. Recalled by...
The Issue: Siemens Healthcare Diagnostics Inc. has confirmed that a negative sodium...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C5-2 Lumify Transducer Probe Recalled by Philips Ultrasound, Inc Due to To...
The Issue: To provide clarification and labelling to define the useful life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S9-2 Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...
The Issue: To provide clarification and labelling to define the useful life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRANSDUCER L12-5 Transducer Probe Recalled by Philips Ultrasound, Inc Due to...
The Issue: To provide clarification and labelling to define the useful life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orascoptic Superior Visualization Dragonfly Essentials Kit ( Nose pad...
The Issue: Due to complaints, loupe nose pads containing nickel may cause an allergic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C6-2 Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...
The Issue: To provide clarification and labelling to define the useful life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: L12-5 38mm Transducer Probe Recalled by Philips Ultrasound, Inc Due to To...
The Issue: To provide clarification and labelling to define the useful life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: C8-4v Transducer Probe Recalled by Philips Ultrasound, Inc Due to To provide...
The Issue: To provide clarification and labelling to define the useful life of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.