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. 2,471 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
2,471 in last 12 months

Showing 3644136460 of 51,434 recalls

Medical DeviceDecember 23, 2015· Xeridiem Mediem Medical Devices Inc

Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00548700 (XMD Recalled by...

The Issue: A feeding () valve leakage issue. The feeding valve appears to close...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2015· Xeridiem Mediem Medical Devices Inc

Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00548770 (XMD Recalled by...

The Issue: A feeding () valve leakage issue. The feeding valve appears to close...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2015· Xeridiem Mediem Medical Devices Inc

Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00548600 (XMD Recalled by...

The Issue: A feeding () valve leakage issue. The feeding valve appears to close...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2015· Xeridiem Mediem Medical Devices Inc

Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00548540 (XMD Recalled by...

The Issue: A feeding () valve leakage issue. The feeding valve appears to close...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2015· Xeridiem Mediem Medical Devices Inc

Recalled Item: EndoVive 3s Low Profile Balloon Kits Part Number: M00549440 (XMD Recalled by...

The Issue: A feeding () valve leakage issue. The feeding valve appears to close...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 23, 2015· Cardinal Scale Mfg Co

Recalled Item: Cardinal Recalled by Cardinal Scale Mfg Co Due to One complaint of a seat on...

The Issue: One complaint of a seat on a scale failing unexpectedly which can cause an...

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

Class II — Potential Health HazardOngoing
DrugDecember 22, 2015· Grato Holdings, Inc.

Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Microbial Contamination of...

The Issue: Microbial Contamination of Non Sterile Products; testing revealed out of...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 22, 2015· Grato Holdings, Inc.

Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Microbial Contamination of...

The Issue: Microbial Contamination of Non Sterile Products; testing revealed out of...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 22, 2015· Grato Holdings, Inc.

Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Microbial Contamination of...

The Issue: Microbial Contamination of Non Sterile Products; testing revealed out of...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 22, 2015· Grato Holdings, Inc.

Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Microbial Contamination of...

The Issue: Microbial Contamination of Non Sterile Products; testing revealed out of...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 22, 2015· Grato Holdings, Inc.

Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Microbial Contamination of...

The Issue: Microbial Contamination of Non Sterile Products; testing revealed out of...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 22, 2015· Grato Holdings, Inc.

Recalled Item: Energique Recalled by Grato Holdings, Inc. Due to Microbial Contamination of...

The Issue: Microbial Contamination of Non Sterile Products; testing revealed out of...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 22, 2015· Bio-Rad Laboratories, Inc.

Recalled Item: EVOLIS Microplate System Recalled by Bio-Rad Laboratories, Inc. Due to The...

The Issue: The error "Washer Reagent Clean Fluid" level low alarmed, which prompted the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2015· Applied Medical Resources Corp

Recalled Item: STD GK258 Recalled by Applied Medical Resources Corp Due to Applied Medical...

The Issue: Applied Medical Resources Corporation is recalling CA500 Epix Universal Clip...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2015· Applied Medical Resources Corp

Recalled Item: STD KIT GK213 Recalled by Applied Medical Resources Corp Due to Applied...

The Issue: Applied Medical Resources Corporation is recalling CA500 Epix Universal Clip...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2015· Ultradent Products, Inc.

Recalled Item: InterGuard 5.5mm Econo Recalled by Ultradent Products, Inc. Due to Ultradent...

The Issue: Ultradent is recalling InterGuard 5.5mm Econo , lot#s BC2GN and BC4L7...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo Plaza Picture archiving and communication system. Software only. PACS...

The Issue: Siemens is releasing an updated software version to address several software...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2015· Applied Medical Resources Corp

Recalled Item: CA500 Epix Universal Clip Applier Product Usage: The Epix disposable...

The Issue: Applied Medical Resources Corporation is recalling CA500 Epix Universal Clip...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2015· Draeger Medical, Inc.

Recalled Item: Emergency Transport Ventilator Oxylog 2000 Plus Ventilator Catalog Number:...

The Issue: Drager became aware of situations where the error message "Poti unplugged"...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 22, 2015· Hospira Inc.

Recalled Item: The Symbiq infusion pump is a device used in a Recalled by Hospira Inc. Due...

The Issue: Potential for the Symbiq pole clamp assemblies to be missing the rubber stop...

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

Class II — Potential Health HazardOngoing