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 2908129100 of 51,434 recalls

DrugJuly 14, 2017· Cantrell Drug Company

Recalled Item: Ephedrine Sulfate Injection Solution 1 mL Recalled by Cantrell Drug Company...

The Issue: Lack of Sterility Assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2017· Cantrell Drug Company

Recalled Item: Succinylcholine Chloride Injection Solution 5 mL Recalled by Cantrell Drug...

The Issue: Lack of Sterility Assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2017· Cantrell Drug Company

Recalled Item: Norepinephrine Bitartrate 16 mg Added to 0.9% Sodium Chloride 250 Recalled...

The Issue: Lack of Sterility Assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2017· Cantrell Drug Company

Recalled Item: Glycopyrrolate Injection Solution Recalled by Cantrell Drug Company Due to...

The Issue: Lack of Sterility Assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2017· SCA Pharmaceuticals

Recalled Item: Potassium Chloride 20 meq Added to Sodium Chloride 0.9% 250 mL Recalled by...

The Issue: Lack of Assurance of Sterility; product has the potential to leak.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2017· SCA Pharmaceuticals

Recalled Item: BUPIVacaine HCl 0.1% PF (From 0.75%) in 0.9% Sodium Chloride Recalled by SCA...

The Issue: Lack of Assurance of Sterility; product has the potential to leak.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2017· SCA Pharmaceuticals

Recalled Item: NORepinephrine 4 mg in 0.9% Sodium Chloride 250 mL from Stock Recalled by...

The Issue: Lack of Assurance of Sterility; product has the potential to leak.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2017· SCA Pharmaceuticals

Recalled Item: BUPIVacaine HCl 0.2% IN 0.9% Sodium Chloride 250 mL Bag Recalled by SCA...

The Issue: Lack of Assurance of Sterility; product has the potential to leak.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2017· Cantrell Drug Company

Recalled Item: Adenosine in 0.9% Sodium Chloride 30mL Recalled by Cantrell Drug Company Due...

The Issue: Lack of Sterility Assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2017· Cantrell Drug Company

Recalled Item: Norepinephrine Bitartrate 8 mg Added to 0.9% Sodium Chloride 250 Recalled by...

The Issue: Lack of Sterility Assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2017· Cantrell Drug Company

Recalled Item: Diltiazem HCl 125 mg in 5% Dextrose 125 mL Single-Dose- Bag Recalled by...

The Issue: Lack of Sterility Assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2017· Cantrell Drug Company

Recalled Item: Norepinephrine Bitartrate 4 mg Added to 0.9% Sodium Chloride 250 Recalled by...

The Issue: Lack of Sterility Assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2017· Cantrell Drug Company

Recalled Item: Ephedrine Sulfate in 0.9% Sodium Chloride 10 mL Recalled by Cantrell Drug...

The Issue: Lack of Sterility Assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 14, 2017· SCA Pharmaceuticals

Recalled Item: PHENYLephrine 20 mg in 0.9% Sodium Chloride 250 mL Bag Recalled by SCA...

The Issue: Lack of Assurance of Sterility; product has the potential to leak.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 14, 2017· Medtronic Inc., Cardiac Rhythm and Heart Failure

Recalled Item: MyCareLink Smart Patient Monitors. It is intended for use with Recalled by...

The Issue: Patients monitored on two (2) or more implanted Medtronic heart devices in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2017· Leica Biosystems Richmond Inc.

Recalled Item: Cell Marque Recalled by Leica Biosystems Richmond Inc. Due to A delay in...

The Issue: A delay in transit may have contributed to nonconformity as the product was...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2017· Leica Biosystems Richmond Inc.

Recalled Item: Cell Marque Recalled by Leica Biosystems Richmond Inc. Due to A delay in...

The Issue: A delay in transit may have contributed to nonconformity as the product was...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2017· Medtronic Inc., Cardiac Rhythm and Heart Failure

Recalled Item: MyCareLink Patient Monitors. It is intended for used with a Recalled by...

The Issue: Patients monitored on two (2) or more implanted Medtronic heart devices in...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2017· Leica Biosystems Richmond Inc.

Recalled Item: Cell Marque Recalled by Leica Biosystems Richmond Inc. Due to A delay in...

The Issue: A delay in transit may have contributed to nonconformity as the product was...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 14, 2017· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: TD60 Transmitter battery charger used with the BeneVision Central Station...

The Issue: A damaged circuit board in the battery charger can cause the battery to...

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

Class II — Potential Health HazardOngoing