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. 2,563 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
2,563 in last 12 months

Showing 1858118600 of 28,964 recalls

Medical DeviceMarch 30, 2017· Smith & Nephew, Inc.

Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...

The Issue: The stability data does not support the product labeled with a 10-year shelf...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Newport Medical Instruments Inc

Recalled Item: Newport Medical HT70 and HT70- Plus Ventilators Recalled by Newport Medical...

The Issue: Medtronic is issuing a voluntary field corrective action for all its...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 30, 2017· Smith & Nephew, Inc.

Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...

The Issue: The stability data does not support the product labeled with a 10-year shelf...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Smith & Nephew, Inc.

Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...

The Issue: The stability data does not support the product labeled with a 10-year shelf...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Smith & Nephew, Inc.

Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...

The Issue: The stability data does not support the product labeled with a 10-year shelf...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Smith & Nephew, Inc.

Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...

The Issue: The stability data does not support the product labeled with a 10-year shelf...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Smith & Nephew, Inc.

Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...

The Issue: The stability data does not support the product labeled with a 10-year shelf...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Breg Inc

Recalled Item: If Hip Recalled by Breg Inc Due to They may not have been sealed prior to...

The Issue: They may not have been sealed prior to sterilization. Products with unsealed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Breg Inc

Recalled Item: Dressing M/U XL Recalled by Breg Inc Due to They may not have been sealed...

The Issue: They may not have been sealed prior to sterilization. Products with unsealed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Breg Inc

Recalled Item: Dressing Shldr XL Recalled by Breg Inc Due to They may not have been sealed...

The Issue: They may not have been sealed prior to sterilization. Products with unsealed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Siemens Medical Solutions USA, Inc.

Recalled Item: 18L6 HD transducer on the ACUSON S Family ultrasound systems Recalled by...

The Issue: When scanning with the 18L6 HD transducer on the ACUSON HELX" Evolution with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Smith & Nephew, Inc.

Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...

The Issue: The stability data does not support the product labeled with a 10-year shelf...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Breg Inc

Recalled Item: Dressing Rect L Recalled by Breg Inc Due to They may not have been sealed...

The Issue: They may not have been sealed prior to sterilization. Products with unsealed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Breg Inc

Recalled Item: Dressing Recalled by Breg Inc Due to They may not have been sealed prior to...

The Issue: They may not have been sealed prior to sterilization. Products with unsealed...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Smith & Nephew, Inc.

Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...

The Issue: The stability data does not support the product labeled with a 10-year shelf...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Smith & Nephew, Inc.

Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...

The Issue: The stability data does not support the product labeled with a 10-year shelf...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Smith & Nephew, Inc.

Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...

The Issue: The stability data does not support the product labeled with a 10-year shelf...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Smith & Nephew, Inc.

Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...

The Issue: The stability data does not support the product labeled with a 10-year shelf...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 30, 2017· Barco N.V.

Recalled Item: Optional MDRC-1119 Front Cover Attachment Kit for review display monitors....

The Issue: If metal strips are removed and re-applied to another display, there is...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 29, 2017· Teleflex Medical

Recalled Item: Arrow EZ-IO Needle Set 45 mm 15 ga Recalled by Teleflex Medical Due to Some...

The Issue: Some of the individual unit packaging (pouches) may be missing the lot...

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

Class III — Low RiskOngoing