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. 2,489 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
2,489 in last 12 months

Showing 3392133940 of 51,434 recalls

Medical DeviceJuly 1, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: Orthopedic manual surgical instrument Usage: Exeter Rasp Handle is a...

The Issue: Malfunctioning of the Exeter Rasp/trial introducer/extractor Handle.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2016· Integra LifeSciences Corp.

Recalled Item: Integra External Fixation System Rocker Bottom Model # 12225400. For...

The Issue: The silicone insert embedded in the rocker bottom has the potential to...

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

Class II — Potential Health HazardOngoing
FoodJuly 1, 2016· Coca-Cola Company (The)

Recalled Item: Huberts Original Lemonade Recalled by Coca-Cola Company (The) Due to Foreign...

The Issue: The product may contain foreign material (glass) in some bottles.

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 1, 2016· Coca-Cola Company (The)

Recalled Item: Huberts Lemonade Strawberry Recalled by Coca-Cola Company (The) Due to...

The Issue: The product may contain foreign material (glass) in some bottles.

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 1, 2016· Coca-Cola Company (The)

Recalled Item: Huberts Lemonade Blackberry Recalled by Coca-Cola Company (The) Due to...

The Issue: The product may contain foreign material (glass) in some bottles.

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

Class II — Potential Health HazardOngoing
Refund
FoodJuly 1, 2016· Coca-Cola Company (The)

Recalled Item: Huberts Lemonade Watermelon Recalled by Coca-Cola Company (The) Due to...

The Issue: The product may contain foreign material (glass) in some bottles.

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 30, 2016· General Mills, Inc

Recalled Item: Case: Beyond Meat Vegetarian Indian Curry with Beyond Chicken Recalled by...

The Issue: General Mills today announced a voluntary recall of a limited quantity of...

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

Class I — Serious Health HazardOngoing
Refund
DrugJune 30, 2016· Allergan Sales, LLC

Recalled Item: TAZORAC (tazarotene) Gel 0.05% Recalled by Allergan Sales, LLC Due to Failed...

The Issue: Failed Content Uniformity Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 30, 2016· Actavis Inc

Recalled Item: Glipizide 2.5 mg Extended-release tablets Recalled by Actavis Inc Due to...

The Issue: Failed Dissolution Specifications: Glipizide 2.5 mg ER Tablets exceeded...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 30, 2016· Allergan Sales, LLC

Recalled Item: TAZORAC (tazarotene) Gel 0.05% Recalled by Allergan Sales, LLC Due to Failed...

The Issue: Failed Content Uniformity Specifications

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 30, 2016· Zimmer Biomet Spine, Inc

Recalled Item: Zyston¿ Transform Instrument Case. Model Number PCR8200-2101. Device labeled...

The Issue: Zimmer Bioment Spine, Inc. announces a voluntary field action for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2016· Zimmer Gmbh

Recalled Item: Avenir M¿ller Stem 4 Standard Avenir M¿ller Stem 6 Lateral Recalled by...

The Issue: Product mix-up. The Avenir M¿ller Stem 6 lateral uncemented might be placed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2016· Zimmer Biomet Spine, Inc

Recalled Item: Zyston¿ Transform Implant Kit. Model Number PCR8200-3101. Device labeled...

The Issue: Zimmer Bioment Spine, Inc. announces a voluntary field action for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2016· Winco Mfg., LLC

Recalled Item: TransMotion Medical Recalled by Winco Mfg., LLC Due to Non-conforming...

The Issue: Non-conforming component caused arms of TMM4 Stretcher chair to no longer...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2016· ARJOHUNTLEIGH POLSKA Sp. z.o.o.

Recalled Item: ArjoHuntleigh Sara Combilizer Recalled by ARJOHUNTLEIGH POLSKA Sp. z.o.o....

The Issue: ArjoHuntleigh has concluded that a device tipping hazard may occur on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2016· TYRX Inc.

Recalled Item: TRYX Antibacterial Envelope Rx Only Product Usage: Indicated for...

The Issue: TRYX products are being recalled since the processes of spaying, welding,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2016· TYRX Inc.

Recalled Item: TRYX Absorbable Antibacterial Envelope Product Usage: Indicated for...

The Issue: TRYX products are being recalled since the processes of spaying, welding,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2016· TYRX Inc.

Recalled Item: TRYX Neuro Absorbable Antibacterial Envelope Product Usage: Indicated for...

The Issue: TRYX products are being recalled since the processes of spaying, welding,...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2016· Winco Mfg., LLC

Recalled Item: TransMotion Medical Recalled by Winco Mfg., LLC Due to Non-conforming...

The Issue: Non-conforming component caused arms of TMM4 Stretcher chair to no longer...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 29, 2016· Winco Mfg., LLC

Recalled Item: TransMotion Medical Recalled by Winco Mfg., LLC Due to Non-conforming...

The Issue: Non-conforming component caused arms of TMM4 Stretcher chair to no longer...

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

Class II — Potential Health HazardOngoing