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 2880128820 of 28,964 recalls

Medical DeviceJanuary 18, 2011· Westmed Inc

Recalled Item: Pulset Arterial Blood Gas (ABG) sampling kit. Full Kit Recalled by Westmed...

The Issue: Westmed is recalling Westmed ABG convenience kits containing TRIAD brand...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 18, 2011· Westmed Inc

Recalled Item: Pulset Arterial Blood Gas (ABG) sampling kit. Full Kit Recalled by Westmed...

The Issue: Westmed is recalling Westmed ABG convenience kits containing TRIAD brand...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 18, 2011· Westmed Inc

Recalled Item: Pulset Arterial Blood Gas (ABG) sampling kit. Modified Kit Recalled by...

The Issue: Westmed is recalling Westmed ABG convenience kits containing TRIAD brand...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 18, 2011· Westmed Inc

Recalled Item: Pulset Arterial Blood Gas (ABG) sampling kit. Modified Kit Recalled by...

The Issue: Westmed is recalling Westmed ABG convenience kits containing TRIAD brand...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 18, 2011· Westmed Inc

Recalled Item: Pulset Arterial Blood Gas (ABG) sampling kit. Full Kit Recalled by Westmed...

The Issue: Westmed is recalling Westmed ABG convenience kits containing TRIAD brand...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 18, 2011· Westmed Inc

Recalled Item: Pulset Arterial Blood Gas (ABG) sampling kit. Modified Kit Recalled by...

The Issue: Westmed is recalling Westmed ABG convenience kits containing TRIAD brand...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 18, 2011· Westmed Inc

Recalled Item: Pulset Arterial Blood Gas (ABG) sampling kit. Full Kit Recalled by Westmed...

The Issue: Westmed is recalling Westmed ABG convenience kits containing TRIAD brand...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 18, 2011· Westmed Inc

Recalled Item: Pulset Arterial Blood Gas (ABG) sampling kit. Full Kit Recalled by Westmed...

The Issue: Westmed is recalling Westmed ABG convenience kits containing TRIAD brand...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 18, 2011· Westmed Inc

Recalled Item: Pulset Arterial Blood Gas (ABG) sampling kit. Full Kit Recalled by Westmed...

The Issue: Westmed is recalling Westmed ABG convenience kits containing TRIAD brand...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 18, 2011· Westmed Inc

Recalled Item: Pulset Arterial Blood Gas (ABG) sampling kit. Modified Kit Recalled by...

The Issue: Westmed is recalling Westmed ABG convenience kits containing TRIAD brand...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 18, 2011· Nemschoff Chairs, Inc.

Recalled Item: Nemschooff Recalled by Nemschoff Chairs, Inc. Due to Nemschoff Chairs, Inc....

The Issue: Nemschoff Chairs, Inc. is recalling various model of the Serenity Treatment...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2011· SteriGear, LLC

Recalled Item: SteriGear Urinary Drain Bag with Fig Leaf Cover Recalled by SteriGear, LLC...

The Issue: SteriGear notifed customers of circumstances in which The Fig Leaf urinary...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2011· Pentax of America Inc

Recalled Item: Video Bronchoscope Recalled by Pentax of America Inc Due to This field...

The Issue: This field action serves to retrospectively document the actions that were...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2011· Pentax of America Inc

Recalled Item: Video Naso pharyngo Laryngoscopes Recalled by Pentax of America Inc Due to...

The Issue: This field action serves to retrospectively document the actions that were...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2011· Pentax of America Inc

Recalled Item: Video Cytoscopes Recalled by Pentax of America Inc Due to This field action...

The Issue: This field action serves to retrospectively document the actions that were...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 1, 2011· Abbott Point Of Care Inc.

Recalled Item: I-STAT EG7+ Cartridge Abbott Point of Care Recalled by Abbott Point Of Care...

The Issue: i-Stat EG7 cartridges may generate falsely depressed PCO2 results for...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 31, 2010· Kimberly-Clark Corporation

Recalled Item: ULTRA Fabric Reinforced Surgical Gown Recalled by Kimberly-Clark Corporation...

The Issue: The impacted product was not intended for commercial distribution to end users.

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

Class III — Low RiskOngoing
Medical DeviceDecember 17, 2010· Philips Electronics North America Corporation

Recalled Item: M3150 Information Center Local Database Recalled by Philips Electronics...

The Issue: Potential for early component failure.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2010· Alphatec Spine, Inc.

Recalled Item: TI Standard Polyaxial Screw Assembly 6.5MM x 55MM. Part # Recalled by...

The Issue: The recall was initiated because Alphatec Spine confirmed that the TI...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2010· Siemens Healthcare Diagnostics, Inc.

Recalled Item: BCS(R) Behring Coagulation System Recalled by Siemens Healthcare...

The Issue: Firm has confirmed that if the Cleaner SCS vial becomes empty after...

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

Class II — Potential Health HazardOngoing