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. 2,614 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
2,614 in last 12 months

Showing 1652116540 of 28,964 recalls

Medical DeviceMarch 26, 2018· Zimmer Biomet, Inc.

Recalled Item: ZMS Intramedullary Fixation Smooth Guide Wire Bullet Tip 3.0 mm Diameter...

The Issue: Potential failure of sterile packaging seal.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2018· Zimmer Biomet, Inc.

Recalled Item: Pressure Sentinel Intramedullary Reaming System Guide Wire Bullet Tip 2.4...

The Issue: Potential failure of sterile packaging seal.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2018· Zimmer Biomet, Inc.

Recalled Item: Zimmer Natural Nail System Tear Drop Guide Wire 2.4 mm Diameter Recalled by...

The Issue: Potential failure of sterile packaging seal.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2018· Zimmer Biomet, Inc.

Recalled Item: ZMS Intramedullary Fixation Smooth Guide Wire 3.0 mm Diameter Recalled by...

The Issue: Potential failure of sterile packaging seal.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2018· Zimmer Biomet, Inc.

Recalled Item: Smooth Guide Wire Bullet Tip 3.0 mm Diameter Recalled by Zimmer Biomet, Inc....

The Issue: Potential failure of sterile packaging seal.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2018· Zimmer Biomet, Inc.

Recalled Item: Zimmer Natural Nail System Tear Drop Guide Wire 3.0 mm Diameter Recalled by...

The Issue: Potential failure of sterile packaging seal.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2018· Zimmer Biomet, Inc.

Recalled Item: ZMS Intramedullary Fixation Smooth Guide Wire 2.4 mm Diameter Recalled by...

The Issue: Potential failure of sterile packaging seal.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2018· Zimmer Biomet, Inc.

Recalled Item: M/DN Intramedullary Fixation Humeral Guide Wire - Smooth 2.4 mm Recalled by...

The Issue: Potential failure of sterile packaging seal.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2018· Zimmer Biomet, Inc.

Recalled Item: Zimmer Natural Nail System Tear Drop Guide Wire 3.0 mm Diameter Recalled by...

The Issue: Potential failure of sterile packaging seal.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2018· Zimmer Biomet, Inc.

Recalled Item: Zimmer Natural Nail System Tear Drop Guide Wire 2.4 mm Diameter Recalled by...

The Issue: Potential failure of sterile packaging seal.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2018· Straumann Manufacturing, Inc.

Recalled Item: Straumann¿ Emdogain 0.7 ml Multipack. Enamel Matrix Derivative. Article...

The Issue: A change regarding the shelf life of a raw material was implemented without...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2018· Straumann Manufacturing, Inc.

Recalled Item: Straumann¿ Emdogain 0.7 ml Multipack USA. Enamel Matrix Derivative. Article...

The Issue: A change regarding the shelf life of a raw material was implemented without...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2018· Straumann Manufacturing, Inc.

Recalled Item: Straumann¿ Emdogain 0.3 ml Multipack USA. Enamel Matrix Derivative. Article...

The Issue: A change regarding the shelf life of a raw material was implemented without...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2018· Medtronic Sofamor Danek USA Inc

Recalled Item: Medtronic ZEVO(TM) Anterior Cervical Plate System SLOT SCREW Recalled by...

The Issue: Slot screw had an overall length of 15mm, but per the specification, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2018· Straumann Manufacturing, Inc.

Recalled Item: Straumann¿ Emdogain 015 Recalled by Straumann Manufacturing, Inc. Due to A...

The Issue: A change regarding the shelf life of a raw material was implemented without...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2018· Medtronic Navigation, Inc.

Recalled Item: Visualase Cooled Laser Applicator System (VCLAS) labeled as: a. Part...

The Issue: Medtronic has become aware that certain lots of the VCLAS 3MM, 10MM, and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2018· Straumann Manufacturing, Inc.

Recalled Item: Straumann¿ Emdogain 0.15 ml 5-Pack. Enamel Matrix Derivative. Article Number...

The Issue: A change regarding the shelf life of a raw material was implemented without...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 23, 2018· Straumann Manufacturing, Inc.

Recalled Item: Straumann¿ Emdogain 0.3 ml Multipack. Enamel Matrix Derivative. Article...

The Issue: A change regarding the shelf life of a raw material was implemented without...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2018· GE Medical Systems Ultrasound & Primary Care Diagnostics, LL

Recalled Item: GE Vivid E7 ultrasound system Product Usage: Vivid E7 is Recalled by GE...

The Issue: The system side of the power cord may break and expose the electrical...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2018· Becton Dickinson & Company

Recalled Item: BD Vacutainer¿ Lithium Heparin Green Top Tube Recalled by Becton Dickinson &...

The Issue: BD Vacutainer EDTA Lavender, Tan, and Pink Top Tubes and BD Vacutainer...

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

Class I — Serious Health HazardOngoing