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 1584115860 of 28,964 recalls

Medical DeviceJuly 12, 2018· Ortho Clinical Diagnostics Inc

Recalled Item: VITROS Immunodiagnostic Products - Folate Reagent Pack(10758750009237)...

The Issue: The recalling firm determined that biased results may occur for specific...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2018· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products Cl- Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: The slides failed to meet current claims for Limit of Blank (LoB), Limit of...

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

Class III — Low RiskOngoing
Medical DeviceJuly 11, 2018· COVIDIEN LLC

Recalled Item: 400mL Recalled by COVIDIEN LLC Due to The temperature sensor catheters may...

The Issue: The temperature sensor catheters may be defective in that they will show a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2018· COVIDIEN LLC

Recalled Item: TEMP SENSE SILICONE 14FR5CC2W Recalled by COVIDIEN LLC Due to The...

The Issue: The temperature sensor catheters may be defective in that they will show a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2018· COVIDIEN LLC

Recalled Item: P400 PREM U/M 18FR TMPSNS Recalled by COVIDIEN LLC Due to The temperature...

The Issue: The temperature sensor catheters may be defective in that they will show a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2018· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products Cl- Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: The slides do not meet the maximum allowable interference (MAI) claims for...

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

Class III — Low RiskOngoing
Medical DeviceJuly 11, 2018· COVIDIEN LLC

Recalled Item: P400 PREM U/M 16FR TMPSNS Recalled by COVIDIEN LLC Due to The temperature...

The Issue: The temperature sensor catheters may be defective in that they will show a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2018· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products Cl- Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: The slides do not meet the maximum allowable interference (MAI) claims for...

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

Class III — Low RiskOngoing
Medical DeviceJuly 11, 2018· COVIDIEN LLC

Recalled Item: 400mL Recalled by COVIDIEN LLC Due to The temperature sensor catheters may...

The Issue: The temperature sensor catheters may be defective in that they will show a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2018· COVIDIEN LLC

Recalled Item: 400mL Recalled by COVIDIEN LLC Due to The temperature sensor catheters may...

The Issue: The temperature sensor catheters may be defective in that they will show a...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 11, 2018· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products CREA Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: The slides did not meet the current claims for Limit of Blank (LoB), Limit...

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

Class III — Low RiskOngoing
Medical DeviceJuly 11, 2018· Spacelabs Healthcare, Ltd.

Recalled Item: Arkon Anesthesia Delivery System with Arkon Software Version 2.70 Recalled...

The Issue: Arkon Anesthesia Delivery System may go into a failed state (mechanical...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 10, 2018· Arrow International Inc

Recalled Item: HANDS-OFF Multi-Lumen Central Venous Catheter with Blue FlexTip for use...

The Issue: The packaging may not be sealed. If the packaging is compromised in this...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2018· Arrow International Inc

Recalled Item: HANDS-OFF Multi-Lumen Central Venous Catheter with Blue FlexTip for use...

The Issue: The packaging may not be sealed. If the packaging is compromised in this...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 10, 2018· Encore Medical, LP

Recalled Item: djosurgical Linear Neck Trials with Spring Sides Recalled by Encore Medical,...

The Issue: The retaining ring on the neck trials has a potential to fail interoperatively.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 9, 2018· Merit Medical Systems, Inc.

Recalled Item: ChloraPrep With Tint Recalled by Merit Medical Systems, Inc. Due to A...

The Issue: A nonsterile bulk product designated for further processing in a tray was...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2018· Smiths Medical ASD Inc.

Recalled Item: smiths medical portex First Breath Nasal Oxygen Cannula Recalled by Smiths...

The Issue: "Manufactured" and "Use By" labels are transposed incorrectly suggesting the...

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

Class III — Low RiskOngoing
Medical DeviceJuly 6, 2018· Smiths Medical ASD Inc.

Recalled Item: smiths medical portex First Breath Adult Nasal Cannula Recalled by Smiths...

The Issue: "Manufactured" and "Use By" labels are transposed incorrectly suggesting the...

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

Class III — Low RiskOngoing
Medical DeviceJuly 6, 2018· Smiths Medical ASD Inc.

Recalled Item: smiths medical portex First Breath Adult Nasal Cannula Recalled by Smiths...

The Issue: "Manufactured" and "Use By" labels are transposed incorrectly suggesting the...

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

Class III — Low RiskOngoing
Medical DeviceJuly 6, 2018· Neotract Inc

Recalled Item: UroLift System Number: UL400-4 Tray Contents: UroLift System Recalled by...

The Issue: Upon implant deployment, the Capsular Tab may not be delivered as the needle...

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

Class II — Potential Health HazardOngoing