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. 2,506 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
2,506 in last 12 months

Showing 3138131400 of 51,434 recalls

FoodMarch 3, 2017· Vulto Creamery

Recalled Item: artisanal cheese VULTO Creamery HANDMADE CHEESE Recalled by Vulto Creamery...

The Issue: Listeria monocytogenes contamination

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 3, 2017· Vulto Creamery

Recalled Item: artisanal cheese VULTO Creamery HANDMADE CHEESE Recalled by Vulto Creamery...

The Issue: Listeria monocytogenes contamination

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 3, 2017· Vulto Creamery

Recalled Item: artisanal cheese VULTO Creamery HANDMADE CHEESE Recalled by Vulto Creamery...

The Issue: Listeria monocytogenes contamination

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 3, 2017· Vulto Creamery

Recalled Item: artisanal cheese VULTO Creamery HANDMADE CHEESE Recalled by Vulto Creamery...

The Issue: Listeria monocytogenes contamination

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 3, 2017· Vulto Creamery

Recalled Item: artisanal cheese VULTO Creamery HANDMADE CHEESE Recalled by Vulto Creamery...

The Issue: Listeria monocytogenes contamination

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMarch 2, 2017· Philips Visicu

Recalled Item: eCare Coordinator Product Usage: is software intended for use in Recalled by...

The Issue: eCareCoordinator (eCC) is intended for use in data aggregation, patient...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 2, 2017· Ortho Kinematics, Inc

Recalled Item: Vertebral Motion Analyzer (VMA) Recalled by Ortho Kinematics, Inc Due to...

The Issue: Ortho Kinematics notified customers that errors were contained in...

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

Class II — Potential Health HazardOngoing
DrugMarch 2, 2017· Fougera Pharmaceuticals Inc.

Recalled Item: Desonide Ointment Recalled by Fougera Pharmaceuticals Inc. Due to Labeling:...

The Issue: Labeling: Label Mixup; Unit boxes labeled as Desonide Ointment 0.05% may...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 1, 2017· Signature Club A Ltd

Recalled Item: Double Hyaluronic 1000 Recalled by Signature Club A Ltd Due to Microbial...

The Issue: Microbial Contamination of Non-Sterile Products: odor complaint of product...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 28, 2017· G & W Laboratories, Inc.

Recalled Item: Clindamycin Phosphate Topical Solution USP Recalled by G & W Laboratories,...

The Issue: CGMP Deviations: an expired active ingredient was used in the manufacture of...

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

Class III — Low RiskOngoing
Refund
Medical DeviceFebruary 28, 2017· Zimmer Biomet, Inc.

Recalled Item: Fem IM Nail 15mmdx48cm Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...

The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2017· Zimmer Biomet, Inc.

Recalled Item: Por fullct fem st 18x200mm Recalled by Zimmer Biomet, Inc. Due to Zimmer...

The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2017· Zimmer Biomet, Inc.

Recalled Item: Fem IM Nail 15mmdx50cm Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...

The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2017· Zimmer Biomet, Inc.

Recalled Item: Xl por st 25.5x220mm Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...

The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2017· Zimmer Biomet, Inc.

Recalled Item: Fem IM Nail 16mmdx44cm Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...

The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2017· Zimmer Biomet, Inc.

Recalled Item: Por fullct fem st 17x200mm Recalled by Zimmer Biomet, Inc. Due to Zimmer...

The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2017· Zimmer Biomet, Inc.

Recalled Item: Segmental fluted stem Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...

The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2017· Zimmer Biomet, Inc.

Recalled Item: Fem IM Nail 14mmdx48cm left Recalled by Zimmer Biomet, Inc. Due to Zimmer...

The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2017· Zimmer Biomet, Inc.

Recalled Item: Fem IM Nail 16mmdx42cm Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...

The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 28, 2017· Zimmer Biomet, Inc.

Recalled Item: Fem IM Nail 16mmdx38cm Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet...

The Issue: Zimmer Biomet Inc. initiated a field action on 02/28/2017 for...

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

Class II — Potential Health HazardOngoing