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 2860128620 of 28,964 recalls

Medical DeviceFebruary 9, 2012· Integra LifeSciences Corp.

Recalled Item: Integra¿ Advansys Medial Lisfranc Plate (MLP) Recalled by Integra...

The Issue: Incorrect technique applied may cause potential rupture of the tibialis...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2012· Covidien LLC dba Uni-Patch

Recalled Item: Reusable Recalled by Covidien LLC dba Uni-Patch Due to Covidien is...

The Issue: Covidien is conducting a voluntary recall regarding specific lots of TENS...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2012· Covidien LLC dba Uni-Patch

Recalled Item: Reusable Recalled by Covidien LLC dba Uni-Patch Due to Covidien is...

The Issue: Covidien is conducting a voluntary recall regarding specific lots of TENS...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2012· Covidien LLC dba Uni-Patch

Recalled Item: Performa reusable and self-adhering TENS/NMES/FES stimulating electrodes...

The Issue: Covidien is conducting a voluntary recall regarding specific lots of TENS...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 9, 2012· Covidien LLC dba Uni-Patch

Recalled Item: Empi STIMC RE Self Adhesive electrodes. For use on TENS Recalled by Covidien...

The Issue: Covidien is conducting a voluntary recall regarding specific lots of TENS...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2012· Afassco Inc

Recalled Item: The finger cots are made out of natural rubber. They Recalled by Afassco Inc...

The Issue: The firm is initiating a field correction because the product(s) were...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2012· Accumetrics Inc

Recalled Item: VerifyNow System Recalled by Accumetrics Inc Due to The recall was initiated...

The Issue: The recall was initiated by Accumetrics because of a field correction to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2012· Metrex Research, LLC.

Recalled Item: CaviCide Recalled by Metrex Research, LLC. Due to Metrex Research is...

The Issue: Metrex Research is recalling Cavicide containing the Spring Fresh Fragrance...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2012· Accumetrics Inc

Recalled Item: VerifyNow P2Y12 Assay Recalled by Accumetrics Inc Due to The recall was...

The Issue: The recall was initiated by Accumetrics because of a field correction to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2012· Hospira Inc.

Recalled Item: Plum A+ Hyperbaric Infusion Pump Recalled by Hospira Inc. Due to Hospira has...

The Issue: Hospira has received reports of distal pressure sensor calibration drift on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2012· Hospira Inc.

Recalled Item: Plum A+ Infusion Pump Recalled by Hospira Inc. Due to Hospira has received...

The Issue: Hospira has received reports of distal pressure sensor calibration drift on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2012· Hospira Inc.

Recalled Item: Plum A+ Infusion Pump Recalled by Hospira Inc. Due to Hospira has received...

The Issue: Hospira has received reports of distal pressure sensor calibration drift on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2012· Hospira Inc.

Recalled Item: *** 1) Plum A+ Infusion Pump Recalled by Hospira Inc. Due to Hospira has...

The Issue: Hospira has received reports of distal pressure sensor calibration drift on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2012· Hospira Inc.

Recalled Item: Plum A+3 Infusion Pump System Recalled by Hospira Inc. Due to Hospira has...

The Issue: Hospira has received reports of distal pressure sensor calibration drift on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2012· Hospira Inc.

Recalled Item: Plum A+ Infusion Pump Recalled by Hospira Inc. Due to Hospira has received...

The Issue: Hospira has received reports of distal pressure sensor calibration drift on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 5, 2012· Hospira Inc.

Recalled Item: Plum A+ Infusion Pump Recalled by Hospira Inc. Due to Hospira has received...

The Issue: Hospira has received reports of distal pressure sensor calibration drift on...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 4, 2012· Orthosensor

Recalled Item: "****ORTHO SENSOR**12-123-A Knee Trial for Trithion***1560 Saw grass...

The Issue: Ortho sensor in Sunrise, FL is recalling the Graphics User Interface...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2012· Roche Molecular Systems, Inc.

Recalled Item: COBAS AmpliPrep Sample Tube Input Barcode Clips Recalled by Roche Molecular...

The Issue: Certain lots of COBAS AmpliPrep (CAP) S-tube Input (Box of 12 bags 12x24...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2012· Abbott Point Of Care Inc.

Recalled Item: i-Stat BNP cartridges Abbott Point of Care Inc. The i-Stat Recalled by...

The Issue: The frequency of suppressed results for i-Stat cTnl, BNP and CK-MP...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 1, 2012· Abbott Point Of Care Inc.

Recalled Item: i-Stat CK-MP cartridges Abbott Point of Care Inc. The i-Stat Recalled by...

The Issue: The frequency of suppressed results for i-Stat cTnl, BNP and CK-MP...

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

Class II — Potential Health HazardOngoing