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. 1,099 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
1,099 in last 12 months

Showing 14281–14300 of 51,434 recalls

Medical DeviceNovember 17, 2021· Beaver Visitec International, Inc.

Recalled Item: Malosa Core Phaco Pack 1-Medical Cataract Kit intended to be Recalled by...

The Issue: Kit packaging may have small holes compromising product sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2021· Beaver Visitec International, Inc.

Recalled Item: Malosa Core LASIK Pack 2-Medical Kit- intended to be Recalled by Beaver...

The Issue: Kit packaging may have small holes compromising product sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2021· Luminex Corporation

Recalled Item: ARIES HSV 1&2 Assay Recalled by Luminex Corporation Due to Impacted lot may...

The Issue: Impacted lot may leak inside the ARIES instrument. Testing confirmed a leak...

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

Class II — Potential Health HazardOngoing
DrugNovember 17, 2021· Sandoz Inc

Recalled Item: Enoxaparin Sodium Injection Recalled by Sandoz Inc Due to Temperature Abuse;...

The Issue: Temperature Abuse; temperature excursion during shipping

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 17, 2021· Blistex Inc

Recalled Item: Odor-Eaters Spray Powder Recalled by Blistex Inc Due to Chemical...

The Issue: Chemical contamination: Presence of benzene

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 16, 2021· Abbott

Recalled Item: Ultimum HEMOSTASIS INTRODUCER 5f 1.67 MM Recalled by Abbott Due to As a...

The Issue: As a result of a manufacturing error, one (1) lot of Ultimum Hemostasis...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 16, 2021· Roche Molecular Systems, Inc.

Recalled Item: cobas LiatSystem Recalled by Roche Molecular Systems, Inc. Due to Roche has...

The Issue: Roche has identified a small number of cobas Liat analyzer units that have...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 16, 2021· Ohio Medical Corporation

Recalled Item: Instavac Portable Suction Pump Recalled by Ohio Medical Corporation Due to...

The Issue: Increase in premature device failures

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 15, 2021· Datascope Corp.

Recalled Item: Cardiosave Hybrid IntraAortic Balloon Pump. Model Numbers: 0998-00-0800-31...

The Issue: Firm is initiating a correction due to the possibility of fluid ingress....

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 15, 2021· Datascope Corp.

Recalled Item: Cardiosave Rescue IntraAortic Balloon Pump. Model Numbers: 0998-00-0800-75...

The Issue: Firm is initiating a correction due to the possibility of fluid ingress....

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

Class I — Serious Health HazardOngoing
DrugNovember 15, 2021· Aurobindo Pharma USA Inc.

Recalled Item: Carvedilol Tablets Recalled by Aurobindo Pharma USA Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
FoodNovember 15, 2021· The Fillo Factory Inc.

Recalled Item: TaDah! FALAFEL STREET WRAP WITH SPICY BROWN SUGAR HARISSA HUMMUS Recalled by...

The Issue: Undeclared milk allergen

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 12, 2021· Dr. Reddy's Laboratories, Inc.

Recalled Item: Antihistamine & Nasal Decongestant Recalled by Dr. Reddy's Laboratories,...

The Issue: Failed dissolution specifications

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

Class III — Low RiskOngoing
Refund
DrugNovember 12, 2021· Dr. Reddy's Laboratories, Inc.

Recalled Item: Allergy & Congestion Fexofenadine HCl 60 mg & Pseudoephedrine HCl Recalled...

The Issue: Failed dissolution specifications

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

Class III — Low RiskOngoing
Refund
DrugNovember 12, 2021· Dr. Reddy's Laboratories, Inc.

Recalled Item: Fexofenadine HCl Recalled by Dr. Reddy's Laboratories, Inc. Due to Failed...

The Issue: Failed dissolution specifications

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

Class III — Low RiskOngoing
Refund
DrugNovember 12, 2021· Dr. Reddy's Laboratories, Inc.

Recalled Item: Allergy & Congestion Relief Allergy Relief D Recalled by Dr. Reddy's...

The Issue: Failed dissolution specifications

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

Class III — Low RiskOngoing
Refund
DrugNovember 12, 2021· Dr. Reddy's Laboratories, Inc.

Recalled Item: Allergy Relief D Fexofenadine HCl Recalled by Dr. Reddy's Laboratories, Inc....

The Issue: Failed dissolution specifications

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

Class III — Low RiskOngoing
Refund
DrugNovember 12, 2021· Dr. Reddy's Laboratories, Inc.

Recalled Item: Fexofenadine HCl 60 mg/ Pseudoephedrine HCl 120 mg Extended Release Recalled...

The Issue: Failed dissolution specifications

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

Class III — Low RiskOngoing
Refund
DrugNovember 12, 2021· Dr. Reddy's Laboratories, Inc.

Recalled Item: Allergy Relief D Fexofenadine HCl Recalled by Dr. Reddy's Laboratories, Inc....

The Issue: Failed dissolution specifications

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

Class III — Low RiskOngoing
Refund
DrugNovember 12, 2021· SterRx, LLC

Recalled Item: MORPHINE SULFATE Recalled by SterRx, LLC Due to Lack of Assurance of Sterility

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund