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. 2,551 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
2,551 in last 12 months

Showing 2062120640 of 51,434 recalls

DrugOctober 22, 2019· Sanofi-Aventis U.S. LLC

Recalled Item: Regular Strength Zantac 75 mg Recalled by Sanofi-Aventis U.S. LLC Due to...

The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 22, 2019· Sanofi-Aventis U.S. LLC

Recalled Item: Zantac 150 mg Recalled by Sanofi-Aventis U.S. LLC Due to CGMP Deviations:...

The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 22, 2019· Sanofi-Aventis U.S. LLC

Recalled Item: Regular Strength Zantac 75 mg Recalled by Sanofi-Aventis U.S. LLC Due to...

The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 22, 2019· Sanofi-Aventis U.S. LLC

Recalled Item: Cool Mint Tablets Maximum Strength Zantac 150 mg Sanofi Distributed by:...

The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 22, 2019· Sanofi-Aventis U.S. LLC

Recalled Item: Maximum Strength Zantac 150 mg Recalled by Sanofi-Aventis U.S. LLC Due to...

The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 22, 2019· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Estradiol Vaginal Inserts USP Recalled by Glenmark Pharmaceuticals Inc., USA...

The Issue: Defective Delivery System: complaints for difficulty in pushing the plunger...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 22, 2019· Sanofi-Aventis U.S. LLC

Recalled Item: Maximum Strength Zantac 150 mg Distributed by: Chattem Recalled by...

The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 22, 2019· Sanofi-Aventis U.S. LLC

Recalled Item: Cool Mint Maximum Strength Zantac 150 mg Recalled by Sanofi-Aventis U.S. LLC...

The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 22, 2019· Sanofi-Aventis U.S. LLC

Recalled Item: Regular Strength Zantac 75 mg Recalled by Sanofi-Aventis U.S. LLC Due to...

The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 22, 2019· Sanofi-Aventis U.S. LLC

Recalled Item: Regular Strength Zantac 150 mg Recalled by Sanofi-Aventis U.S. LLC Due to...

The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 22, 2019· Sanofi-Aventis U.S. LLC

Recalled Item: Zantac 75 mg Recalled by Sanofi-Aventis U.S. LLC Due to CGMP Deviations:...

The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 22, 2019· Sanofi-Aventis U.S. LLC

Recalled Item: Regular Strength Zantac 150 mg Distributed by: Chattem Recalled by...

The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 22, 2019· Steris Corporation

Recalled Item: Eagle 3000 Sterilizer Recalled by Steris Corporation Due to Potential for...

The Issue: Potential for the incorrect pressure safety valve being included in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2019· Edwards Lifesciences, LLC

Recalled Item: EZ Glide Aortic Cannula Recalled by Edwards Lifesciences, LLC Due to Their...

The Issue: Their is a possibility that the cannula may separate from its connector,...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2019· Steris Corporation

Recalled Item: Evolution Loading Car and Transfer Carriage- Accessory to the Sterilizer...

The Issue: The locking pin of the front wheel asse mbly of the Evolution Transfer...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 22, 2019· Encore Medical, LP

Recalled Item: EMPOWR Acetabular System Recalled by Encore Medical, LP Due to The firm...

The Issue: The firm received complaints that the EMPOWR Acetabular Impactor Balls were...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Haemonetics Corporation

Recalled Item: CS Elite Fastpack Recalled by Haemonetics Corporation Due to Potential to...

The Issue: Potential to develop leaks at the inner core of Cell Saver¿ 5/5+ and Cell...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Integra LifeSciences Corp.

Recalled Item: C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System Recalled by Integra...

The Issue: The 36 kHz Sterilization Tray (C7136 Rev C / 72904491 Rev A) system does not...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Integra LifeSciences Corp.

Recalled Item: C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System Recalled by Integra...

The Issue: The 36 kHz Sterilization Tray (C7136 Rev C / 72904491 Rev A) system does not...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 21, 2019· Integra LifeSciences Corp.

Recalled Item: C7000 - CUSA¿ Clarity Ultrasonic Tissue Ablation System Recalled by Integra...

The Issue: The 36 kHz Sterilization Tray (C7136 Rev C / 72904491 Rev A) system does not...

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

Class II — Potential Health HazardOngoing