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. 2,489 recalls have been distributed to Colorado in the last 12 months.
Showing 34401–34420 of 51,434 recalls
Recalled Item: Pediatric ThermoGard¿ Dual Dispersive Electrodes (for patients 5-15 kg.)...
The Issue: A version of the dual dispersive electrodes may not be compatible with some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adult ThermoGard¿ Dual Dispersive Electrodes (for patients >15 kg.) Recalled...
The Issue: A version of the dual dispersive electrodes may not be compatible with some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Adult Dual Dispersive Electrodes (for patients >15 kg.) Recalled by Conmed...
The Issue: A version of the dual dispersive electrodes may not be compatible with some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pediatric Dual Dispersive Electrodes (for patients 5-15 kg.) Recalled by...
The Issue: A version of the dual dispersive electrodes may not be compatible with some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products Ca Slides Recalled by Ortho-Clinical Diagnostics...
The Issue: Ortho Clinical Diagnostics (OCD) confirmed a potential for biased calcium...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monaco RTP System Product Usage: The Monaco system is used Recalled by...
The Issue: When DICOM exporting a 3D Monaco plan and the "Composite Field Sequencing"...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15 Recalled by...
The Issue: Subpotent Drug: Two of the active sunscreen ingredients, octinoxate and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15 Recalled by...
The Issue: Subpotent Drug: Two of the active sunscreen ingredients, octinoxate and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15 Recalled by...
The Issue: Subpotent Drug: Two of the active sunscreen ingredients, octinoxate and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15 Recalled by...
The Issue: Subpotent Drug: Two of the active sunscreen ingredients, octinoxate and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15 Recalled by...
The Issue: Subpotent Drug: Two of the active sunscreen ingredients, octinoxate and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CLINIQUE moisture surge tinted moisturizer broad spectrum SPF 15 Recalled by...
The Issue: Subpotent Drug: Two of the active sunscreen ingredients, octinoxate and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sulfacetamide Sodium Ophthalmic Solution Recalled by Akorn, Inc. Due to Lack...
The Issue: Lack of Assurance of Sterility; some lots failed Antimicrobial Effectiveness...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Calix T PEEK Lumbar System Recalled by X Spine Systems Inc Due to The trials...
The Issue: The trials and rasps used to prepare the surgical site for placement of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Calix P PEEK Lumbar System Recalled by X Spine Systems Inc Due to The trials...
The Issue: The trials and rasps used to prepare the surgical site for placement of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Calix P PEEK Lumbar System Recalled by X Spine Systems Inc Due to The trials...
The Issue: The trials and rasps used to prepare the surgical site for placement of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Calix T PEEK Lumbar System Recalled by X Spine Systems Inc Due to The trials...
The Issue: The trials and rasps used to prepare the surgical site for placement of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista¿ Homocysteine Flex Reagent Cartridge (HCYS) Recalled by CSL...
The Issue: Reagent lots # 15243MA and 15243MB shows a reduced stability once opened...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gas Delivery Engine (GDE) Recalled by Carefusion 211 Inc dba Carefusion Due...
The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gas Delivery Engine (GDE)- Recalled by Carefusion 211 Inc dba Carefusion Due...
The Issue: CareFusion has identified a potential risk associated with AVEA Ventilator...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.