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. 2,509 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
2,509 in last 12 months

Showing 2692126940 of 28,964 recalls

Medical DeviceMarch 31, 2013· Sysmex America, Inc.

Recalled Item: The UF-1000i is a fully automated urine particle analyzer intended Recalled...

The Issue: The current Century Break patch did not contain the same setting for the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2013· Cordis Corporation

Recalled Item: Cordis OPTEASE Retrieval Inferior Vena Cava (IVC) Filter***. No.***466F220A...

The Issue: Correction to provide clarification and additional labeling to minimize...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 28, 2013· Abbott Molecular

Recalled Item: The CEP 8 SpectrumGreen (SG) ASR Probe Kit Recalled by Abbott Molecular Due...

The Issue: 20 kits of CEP 8 SG ASR Probe (list 06J37-018, lot 440023), contained Vysis...

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

Class III — Low RiskOngoing
Medical DeviceMarch 28, 2013· Custom Spine, Inc.

Recalled Item: Custom Spine ISSYS LP Inverted Screw System. 8.5MM X 45 Recalled by Custom...

The Issue: On March 28, 2013, Custom Spine, Inc. issued a minor removal of a lot of 18...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Elekta, Inc.

Recalled Item: Integrity 1.1. Integrity is the interface and control software for Recalled...

The Issue: The problem is that the "static tolerances" from the calibration files...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Smiths Medical ASD, Inc.

Recalled Item: Wallace Sure-Pro¿ Two Stage Embryo Replacement Catheter with Obturator...

The Issue: Unable to pass catheter through outer sheath during embryo transfer

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Integra LifeSciences Corporation

Recalled Item: Absorbable Collagen Sponge Provided As Intermediate to Another Company...

The Issue: Due to the process deviation, product lots in question may have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Integra LifeSciences Corporation

Recalled Item: CollaPlug Absorbable Collagen Wound Dressing for Dental Surgery The...

The Issue: Due to the process deviation, product lots in question may have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Smiths Medical ASD, Inc.

Recalled Item: Wallace Sure-Pro¿ Two Stage Embryo Replacement Catheter for difficult...

The Issue: Unable to pass catheter through outer sheath during embryo transfer

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Baxter Healthcare Corp.

Recalled Item: A) Product Code 2N3371: Non-DEHP Y-Type Catheter Extension Set Recalled by...

The Issue: Customers have reported that when separating an individual package from its...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· GE Healthcare, LLC

Recalled Item: Optima MR430s MRI Scanner Recalled by GE Healthcare, LLC Due to Coolant...

The Issue: Coolant supply lines may leak liquid onto the floor resulting in a slippery...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· GE Healthcare, LLC

Recalled Item: MSK EXTREME MR SCANNER Recalled by GE Healthcare, LLC Due to Coolant supply...

The Issue: Coolant supply lines may leak liquid onto the floor resulting in a slippery...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Baxter Healthcare Corp.

Recalled Item: A) Product Code 2N1191: Non-DEHP Y-Type Catheter Extension Set Recalled by...

The Issue: Customers have reported that when separating an individual package from its...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Integra LifeSciences Corporation

Recalled Item: Helistat Absorbable Hemostatic Recalled by Integra LifeSciences Corporation...

The Issue: Due to the process deviation, product lots in question may have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Integra LifeSciences Corporation

Recalled Item: HeliPlug Absorbable Collagen Wound Dressing for Dental Surgery The...

The Issue: Due to the process deviation, product lots in question may have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Stryker Howmedica Osteonics Corp.

Recalled Item: Stryker Howmedica Osteonics Corp. AxSOS System Instrument. The AxSOS Locking...

The Issue: Stryker Orthopaedics has received a report indicating that the scale of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Smiths Medical ASD, Inc.

Recalled Item: Wallace Sure-Pro Ultra¿ Embryo Replacement Catheter with Stylet Product...

The Issue: Unable to pass catheter through outer sheath during embryo transfer

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Integra LifeSciences Corporation

Recalled Item: Colla Tape Absorbable Collagen Wound Dressing for Dental Surgery The...

The Issue: Due to the process deviation, product lots in question may have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Baxter Healthcare Corp.

Recalled Item: A) Product Code 2N8371: Non-DEHP Y-Type Catheter Extension Set Kit Recalled...

The Issue: Customers have reported that when separating an individual package from its...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2013· Integra LifeSciences Corporation

Recalled Item: INSTAT - Agent Recalled by Integra LifeSciences Corporation Due to Due to...

The Issue: Due to the process deviation, product lots in question may have been...

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

Class II — Potential Health HazardOngoing