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. 2,509 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
2,509 in last 12 months

Showing 2740127420 of 51,434 recalls

FoodFebruary 14, 2018· Springside Cheese Corp

Recalled Item: Springside Monterey Jack Pueblo Cheese packaged in the following sizes:...

The Issue: Various cheeses are being recalled because they may have been made with milk...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
FoodFebruary 14, 2018· Springside Cheese Corp

Recalled Item: Springside Monterey Jack Ghost Pepper Cheese packaged in the following...

The Issue: Various cheeses are being recalled because they may have been made with milk...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
FoodFebruary 14, 2018· Springside Cheese Corp

Recalled Item: Springside Monterey Jack Tomato Basil Cheese Recalled by Springside Cheese...

The Issue: Various cheeses are being recalled because they may have been made with milk...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
FoodFebruary 14, 2018· Springside Cheese Corp

Recalled Item: Springside Monterey Jack Cheese Packaged in the following sizes: Net Wt. 8...

The Issue: Various cheeses are being recalled because they may have been made with milk...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
Medical DeviceFebruary 14, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: ONCOR Expression Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Control Console software has been updated to reduce the risk for collision...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: MEVATRON M2 / PRIMUS Mid-Energy Recalled by Siemens Medical Solutions USA,...

The Issue: Control Console software has been updated to reduce the risk for collision...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: ONCOR Impression Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Control Console software has been updated to reduce the risk for collision...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: ONCOR Avant-garde Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Control Console software has been updated to reduce the risk for collision...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: ONCOR Impression Plus Recalled by Siemens Medical Solutions USA, Inc Due to...

The Issue: Control Console software has been updated to reduce the risk for collision...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 14, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: PRIMUS HI Recalled by Siemens Medical Solutions USA, Inc Due to Control...

The Issue: Control Console software has been updated to reduce the risk for collision...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugFebruary 14, 2018· Fagron, Inc

Recalled Item: SyrSpend SF Suspending Base Recalled by Fagron, Inc Due to Microbial...

The Issue: Microbial contamination of Non-Sterile Product; product contamination with...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 13, 2018· Nostrum Laboratories Inc

Recalled Item: Calcium Acetate Capsules Recalled by Nostrum Laboratories Inc Due to...

The Issue: Presence of Foreign Tablets/Capsules

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugFebruary 13, 2018· Hetero Labs Limited Unit V

Recalled Item: Valganciclovir Tablets Recalled by Hetero Labs Limited Unit V Due to...

The Issue: Temperature Abuse: Valganciclovir Tablets USP 450 mg and Valacyclovir...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 13, 2018· Hetero Labs Limited Unit V

Recalled Item: Valacyclovir Tablets USP 1 gram Recalled by Hetero Labs Limited Unit V Due...

The Issue: Temperature Abuse: Valganciclovir Tablets USP 450 mg and Valacyclovir...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 13, 2018· Tosoh Bioscience Inc

Recalled Item: ST AIA-PACK¿ PROG II Recalled by Tosoh Bioscience Inc Due to Falsely...

The Issue: Falsely elevated progesterone assay values will occur when using certain...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 13, 2018· Becton Dickinson & Company

Recalled Item: BD VACUTAINER PLUS SST Tube with HEMOGARD closure 13x100mm 5.0ml PLBL Gold...

The Issue: Tubes may exhibit stopper creepout/pullout, where the stopper dissociates...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 13, 2018· Becton Dickinson & Company

Recalled Item: BD VACUTAINER PLUS SST Tube with HEMOGARD closure 13x75mm 3.5ml PLBL Gold...

The Issue: Tubes may exhibit stopper creepout/pullout, where the stopper dissociates...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 13, 2018· Tosoh Bioscience Inc

Recalled Item: ST AIA-PACK¿ PROG III Recalled by Tosoh Bioscience Inc Due to Falsely...

The Issue: Falsely elevated progesterone assay values will occur when using certain...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 13, 2018· Stanbio Laboratory, LP

Recalled Item: RaPET¿ RF Latex Reagent used as a component in the Recalled by Stanbio...

The Issue: All patient serum samples yield a weakly positive test result.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 13, 2018· Pentax of America Inc

Recalled Item: Pentax Video Duodenoscope Model: ED-3490TK (UDI of design being recalled:...

The Issue: The duodenoscopes are being recalled in order to replace the forceps...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing