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. 1,133 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
1,133 in last 12 months

Showing 10781–10800 of 28,964 recalls

Medical DeviceNovember 18, 2020· Boston Scientific Corporation

Recalled Item: IcePearl" 2.1 CX Prostate Cryoablation Kit Recalled by Boston Scientific...

The Issue: Complaint trend regarding needle shaft gas leaks.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2020· Boston Scientific Corporation

Recalled Item: IceSeed" 1.5¿ MRI 90¿ Cryoablation Needle ¿ Recalled by Boston Scientific...

The Issue: Complaint trend regarding needle shaft gas leaks.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2020· Boston Scientific Corporation

Recalled Item: IceSphere" 1.5 90¿ Cryoablation Needle Recalled by Boston Scientific...

The Issue: Complaint trend regarding needle shaft gas leaks.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2020· Becton Dickinson & Company

Recalled Item: BD PrecisionGlide Needle 30G x 1/2 (0.3 mm X 13mm) Recalled by Becton...

The Issue: BD has confirmed the presence of blood on the cannulas of the BD...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2020· Shimadzu Medical Systems

Recalled Item: MH-200S Recalled by Shimadzu Medical Systems Due to The firm has identified...

The Issue: The firm has identified a problem with the control software for the celling...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 18, 2020· Aesculap Implant Systems LLC

Recalled Item: ENNOVATE MIS REMOVALKEY SHORT Recalled by Aesculap Implant Systems LLC Due...

The Issue: Fracture or breakage of the spinal fixation arm at the downtube instrument...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2020· Boston Scientific Corporation

Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...

The Issue: Failure to execute the visual inspection correctly prior to locking the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 17, 2020· Zimmer Biomet, Inc.

Recalled Item: Polaris 5.5 Spinal System and Polaris 5.5/Cypher Spinal System Recalled by...

The Issue: Zimmer Biomet is conducting a medical device correction to update the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2020· Boston Scientific Corporation

Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...

The Issue: Failure to execute the visual inspection correctly prior to locking the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 17, 2020· Boston Scientific Corporation

Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...

The Issue: Failure to execute the visual inspection correctly prior to locking the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 17, 2020· Boston Scientific Corporation

Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...

The Issue: Failure to execute the visual inspection correctly prior to locking the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 17, 2020· Remote Diagnostic Technologies Ltd.

Recalled Item: Tempus LS - Manual Defibrillator Recalled by Remote Diagnostic Technologies...

The Issue: A software error was detected within software version 1.3.4 for the Tempus...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 17, 2020· Boston Scientific Corporation

Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...

The Issue: Failure to execute the visual inspection correctly prior to locking the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 17, 2020· Boston Scientific Corporation

Recalled Item: Lotus Edge Valve System Recalled by Boston Scientific Corporation Due to...

The Issue: Failure to execute the visual inspection correctly prior to locking the...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 16, 2020· Boston Scientific Corporation

Recalled Item: Contour VL Variable Length Ureteral Stent Set Recalled by Boston Scientific...

The Issue: Trace amounts of metallic debris were found on the stent related to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 16, 2020· Boston Scientific Corporation

Recalled Item: Contour VL Variable Length Ureteral Stent Recalled by Boston Scientific...

The Issue: Trace amounts of metallic debris were found on the stent related to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 16, 2020· Covidien Llc

Recalled Item: Capnostream 35 Portable Respiratory Monitor Recalled by Covidien Llc Due to...

The Issue: The firm has released software update V01.05.02.16 (also known as V1.5.2) in...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 13, 2020· Randox Laboratories Ltd.

Recalled Item: Randox Rx Series Mg - Product Usage: For the quantitative Recalled by Randox...

The Issue: Failing to meet the linearity performance claims quoted on the kit...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 13, 2020· Randox Laboratories Ltd.

Recalled Item: Randox Mg R1 - Product Usage: For the quantitative in Recalled by Randox...

The Issue: Failing to meet the linearity performance claims quoted on the kit...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 12, 2020· Biocomposites, Ltd.

Recalled Item: Stimulan Kit 10cc Recalled by Biocomposites, Ltd. Due to Mislabeling

The Issue: The product is mislabeled.

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

Class II — Potential Health HazardOngoing