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. 1,794 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
1,794 in last 12 months

Showing 3976139780 of 51,434 recalls

Medical DeviceApril 16, 2015· Biomet, Inc.

Recalled Item: Comprehensive Shoulder System Recalled by Biomet, Inc. Due to Biomet hip...

The Issue: Biomet hip joint, knee joint and shoulder joint replacement components...

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

Class III — Low RiskOngoing
Medical DeviceApril 16, 2015· Biomet, Inc.

Recalled Item: Biomet Cobalt-Chrome Femoral Components Recalled by Biomet, Inc. Due to...

The Issue: Biomet hip joint, knee joint and shoulder joint replacement components...

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

Class III — Low RiskOngoing
Medical DeviceApril 16, 2015· Biomet, Inc.

Recalled Item: Mallory/Head Primary Hip System Recalled by Biomet, Inc. Due to Biomet hip...

The Issue: Biomet hip joint, knee joint and shoulder joint replacement components...

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

Class III — Low RiskOngoing
Medical DeviceApril 16, 2015· Covidien LLC

Recalled Item: Surgical Kit Sterile-Kits containing the Devon Light Glove Catalog...

The Issue: Devon Light Gloves contain splits or holes compromising the sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2015· Biomet, Inc.

Recalled Item: MCK Maximum Congruent Knee System Recalled by Biomet, Inc. Due to Biomet hip...

The Issue: Biomet hip joint, knee joint and shoulder joint replacement components...

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

Class III — Low RiskOngoing
Medical DeviceApril 16, 2015· Covidien LLC

Recalled Item: NS-3600-B LITE GLOVE 1000/CASE -Bulk Recalled by Covidien LLC Due to Devon...

The Issue: Devon Light Gloves contain splits or holes compromising the sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2015· Covidien LLC

Recalled Item: Delivery/C-Section Recalled by Covidien LLC Due to Devon Light Gloves...

The Issue: Devon Light Gloves contain splits or holes compromising the sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2015· Hitachi Medical Systems America Inc

Recalled Item: Hitachi Echelon MRI System Recalled by Hitachi Medical Systems America Inc...

The Issue: Image data transferred from the MRI system to a workstation showed errors on...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2015· Hitachi Medical Systems America Inc

Recalled Item: Hitachi Oasis MRI System Recalled by Hitachi Medical Systems America Inc Due...

The Issue: Image data transferred from the MRI system to a workstation showed errors on...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 16, 2015· Hitachi Medical Systems America Inc

Recalled Item: Hitachi Echelon Oval MRI System Recalled by Hitachi Medical Systems America...

The Issue: Image data transferred from the MRI system to a workstation showed errors on...

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

Class II — Potential Health HazardOngoing
DrugApril 15, 2015· Sandoz, Inc

Recalled Item: Cetirizine HCl Chewable Tablet Recalled by Sandoz, Inc Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: An out of specification (OOS)...

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

Class III — Low RiskOngoing
Refund
DrugApril 15, 2015· Reckitt Benckiser LLC

Recalled Item: Mucinex Fast Max DM Max Recalled by Reckitt Benckiser LLC Due to Labeling:...

The Issue: Labeling: Label Mix-Up; Bottles of Mucinex Fast-Max liquid are correctly...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 15, 2015· Reckitt Benckiser LLC

Recalled Item: Mucinex Fast Max Day Time Severe Cold and Fast-Max Night Recalled by Reckitt...

The Issue: Labeling: Label Mix-Up; Bottles of Mucinex Fast-Max liquid are correctly...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 15, 2015· Reckitt Benckiser LLC

Recalled Item: Mucinex Fast Max Day Time Severe Congestion & Cough Night Time Cold & Flu...

The Issue: Labeling: Label Mix-Up; Bottles of Mucinex Fast-Max liquid are correctly...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 15, 2015· Reckitt Benckiser LLC

Recalled Item: Mucinex Fast Max Severe Congestion & Cough Recalled by Reckitt Benckiser LLC...

The Issue: Labeling: Label Mix-Up; Bottles of Mucinex Fast-Max liquid are correctly...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 15, 2015· Reckitt Benckiser LLC

Recalled Item: Mucinex Fast-Max Cold & Sinus Recalled by Reckitt Benckiser LLC Due to...

The Issue: Labeling: Label Mix-Up; Bottles of Mucinex Fast-Max liquid are correctly...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 15, 2015· Reckitt Benckiser LLC

Recalled Item: Mucinex Fast Max Night Time Cold & Flu Recalled by Reckitt Benckiser LLC Due...

The Issue: Labeling: Label Mix-Up; Bottles of Mucinex Fast-Max liquid are correctly...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 15, 2015· Reckitt Benckiser LLC

Recalled Item: Mucinex Fast Max Cold Recalled by Reckitt Benckiser LLC Due to Labeling:...

The Issue: Labeling: Label Mix-Up; Bottles of Mucinex Fast-Max liquid are correctly...

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 15, 2015· Reaction Nutrition LLC

Recalled Item: Bio Armor Carno Pump Plus Electrolytes 40 servings (Cherry Lime) Recalled by...

The Issue: Work out support nutritional supplements manufactured on shared equipment...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 15, 2015· Reaction Nutrition LLC

Recalled Item: REACTION RECOR: Amino Action- 500g (Cherry Lime) Recalled by Reaction...

The Issue: Work out support nutritional supplements manufactured on shared equipment...

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

Class II — Potential Health HazardOngoing
Refund