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. 2,506 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
2,506 in last 12 months

Showing 3108131100 of 51,434 recalls

Medical DeviceMarch 28, 2017· Aesculap Implant Systems LLC

Recalled Item: GE426R Recalled by Aesculap Implant Systems LLC Due to Foreign Object...

The Issue: Diamond particulates may break off the burr and fall into the surgical site....

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2017· Aesculap Implant Systems LLC

Recalled Item: GP321R Recalled by Aesculap Implant Systems LLC Due to Foreign Object...

The Issue: Diamond particulates may break off the burr and fall into the surgical site....

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2017· Aesculap Implant Systems LLC

Recalled Item: GP161R Recalled by Aesculap Implant Systems LLC Due to Foreign Object...

The Issue: Diamond particulates may break off the burr and fall into the surgical site....

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2017· Bard Peripheral Vascular Inc

Recalled Item: MR GHIATAS Beaded Breast Localization Wire Recalled by Bard Peripheral...

The Issue: It may be at risk of containing a non-MR compatible GHIATAS Beaded Breast...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2017· Draegar Medical Systems, Inc.

Recalled Item: Delta Recalled by Draegar Medical Systems, Inc. Due to It was reported that...

The Issue: It was reported that a set low O2 alarm does not go off although the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2017· Draegar Medical Systems, Inc.

Recalled Item: Delta XL Recalled by Draegar Medical Systems, Inc. Due to It was reported...

The Issue: It was reported that a set low O2 alarm does not go off although the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2017· Draegar Medical Systems, Inc.

Recalled Item: Kappa Recalled by Draegar Medical Systems, Inc. Due to It was reported that...

The Issue: It was reported that a set low O2 alarm does not go off although the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 27, 2017· Alcon Research, Ltd.

Recalled Item: Alcon Patient Care Kits Product Usage: A Patient Care Kit Recalled by Alcon...

The Issue: Alcon is initiating a Voluntary Medical Device Removal because the product...

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

Class II — Potential Health HazardOngoing
DrugMarch 24, 2017· Qinhuangdao Zizhu Pharmaceutical, Co.

Recalled Item: Estriol Micronized Recalled by Qinhuangdao Zizhu Pharmaceutical, Co. Due to...

The Issue: cGMP Deviations; lack of quality assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 24, 2017· Qinhuangdao Zizhu Pharmaceutical, Co.

Recalled Item: Testosterone Micronized Recalled by Qinhuangdao Zizhu Pharmaceutical, Co....

The Issue: cGMP Deviations; lack of quality assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 24, 2017· Qinhuangdao Zizhu Pharmaceutical, Co.

Recalled Item: Estradiol Micronized Bulk Recalled by Qinhuangdao Zizhu Pharmaceutical, Co....

The Issue: cGMP Deviations; lack of quality assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 24, 2017· Qinhuangdao Zizhu Pharmaceutical, Co.

Recalled Item: Estrone Micronized Recalled by Qinhuangdao Zizhu Pharmaceutical, Co. Due to...

The Issue: cGMP Deviations; lack of quality assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 24, 2017· Qinhuangdao Zizhu Pharmaceutical, Co.

Recalled Item: Estradiol Non-Micronized Recalled by Qinhuangdao Zizhu Pharmaceutical, Co....

The Issue: cGMP Deviations; lack of quality assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 24, 2017· Qinhuangdao Zizhu Pharmaceutical, Co.

Recalled Item: Ethinyl Estradiol Micronized Recalled by Qinhuangdao Zizhu Pharmaceutical,...

The Issue: cGMP Deviations; lack of quality assurance.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 24, 2017· Qinhuangdao Zizhu Pharmaceutical, Co.

Recalled Item: Levonorgestrel Non-Micronized Recalled by Qinhuangdao Zizhu Pharmaceutical,...

The Issue: cGMP Deviations; lack of quality assurance.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 24, 2017· Craftmatic Industries, Inc.

Recalled Item: Craftmatic Model 1 Base for Dual Bed Configurations Recalled by Craftmatic...

The Issue: A potential for dual-configured beds to separate or slip away from one another.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2017· Craftmatic Industries, Inc.

Recalled Item: Legacy Base for Dual Bed Configurations Recalled by Craftmatic Industries,...

The Issue: A potential for dual-configured beds to separate or slip away from one another.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2017· Arthrex, Inc.

Recalled Item: Anthrex Bio-SwiveLock SP Vented Recalled by Arthrex, Inc. Due to Some...

The Issue: Some eyelets broke from SwiveLock Anchor on insertion.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2017· Arthrex, Inc.

Recalled Item: Anthrex SpeedBridge Implant System with BioComposite SwiveLock SP Vented...

The Issue: Some eyelets broke from SwiveLock Anchor on insertion.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2017· Arthrex, Inc.

Recalled Item: Anthrex PEEK SwiveLock SP Vented Recalled by Arthrex, Inc. Due to Some...

The Issue: Some eyelets broke from SwiveLock Anchor on insertion.

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

Class II — Potential Health HazardOngoing