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 3702137040 of 51,434 recalls

FoodNovember 4, 2015· Tate's Wholesale, Llc.

Recalled Item: TATE'S BAKE SHOP CHOCOLATE CHIP COOKIES Recalled by Tate's Wholesale, Llc....

The Issue: Tate's Bake Shop has recalled Chocolate Chip Cookies and Ginger Zinger...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
FoodNovember 4, 2015· Tate's Wholesale, Llc.

Recalled Item: TATE'S BAKE SHOP Cookies GINGER ZINGER GLUTEN FREE Recalled by Tate's...

The Issue: Tate's Bake Shop has recalled Chocolate Chip Cookies and Ginger Zinger...

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 3, 2015· Philips Electronics North America Corporation

Recalled Item: Allura Xper FD20 Recalled by Philips Electronics North America Corporation...

The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· bioMerieux, Inc.

Recalled Item: MYLA MASTER DVD 3.2 CLI DL380 Product Usage: MYLA is Recalled by bioMerieux,...

The Issue: MYLA¿ software connected to a Laboratory Information System (LIS) and a...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· Philips Electronics North America Corporation

Recalled Item: Cardiovascular Allura Centron Recalled by Philips Electronics North America...

The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· Philips Electronics North America Corporation

Recalled Item: Allura Xper FD20 Biplane OR Table Recalled by Philips Electronics North...

The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5 Recalled by Ortho-Clinical Diagnostics Due to Software anomaly may...

The Issue: Software anomaly may allow VITROS Systems to sample and process assays while...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· Philips Electronics North America Corporation

Recalled Item: Allura CV20 Recalled by Philips Electronics North America Corporation Due to...

The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· Philips Electronics North America Corporation

Recalled Item: INTEGRIS H3000 Recalled by Philips Electronics North America Corporation Due...

The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· Philips Electronics North America Corporation

Recalled Item: INTEGRIS BN/BV3000 Recalled by Philips Electronics North America Corporation...

The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· Ortho-Clinical Diagnostics

Recalled Item: VITROS 4600 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...

The Issue: Software anomaly may allow VITROS Systems to sample and process assays while...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· Ortho-Clinical Diagnostics

Recalled Item: VITROS 3600 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...

The Issue: Software anomaly may allow VITROS Systems to sample and process assays while...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5600 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...

The Issue: Software anomaly may allow VITROS Systems to sample and process assays while...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· AngioDynamics Inc.

Recalled Item: NAMIC CONVENIENCE KIT SELF REGIONAL HEALTHCARE PV LEG PACK Recalled by...

The Issue: Procedure Products initiated the recall due to the inner lumen of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· Philips Electronics North America Corporation

Recalled Item: Allura Xper FD20/20 Recalled by Philips Electronics North America...

The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· AngioDynamics Inc.

Recalled Item: NAMIC CONVENIENCE KIT MERCY GENERAL HOSPITAL NEURO KIT Recalled by...

The Issue: Procedure Products initiated the recall due to the inner lumen of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· AngioDynamics Inc.

Recalled Item: NAMIC CONVENIENCE KIT HOLYOKE HOSPITAL SPECIAL PROCEDURE KIT Recalled by...

The Issue: Procedure Products initiated the recall due to the inner lumen of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· AngioDynamics Inc.

Recalled Item: NAMIC CONVENIENCE KIT RENOWN REGIONAL MEDICAL CENTER Recalled by...

The Issue: Procedure Products initiated the recall due to the inner lumen of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· bioMerieux, Inc.

Recalled Item: MYLA MASTER DVD V4.0 CLI Product Usage: MYLA is a Recalled by bioMerieux,...

The Issue: MYLA¿ software connected to a Laboratory Information System (LIS) and a...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 3, 2015· Philips Electronics North America Corporation

Recalled Item: UNIQ FD OR table Recalled by Philips Electronics North America Corporation...

The Issue: The use of Allura Xper, Allura Clarity, Allura CV, Allura Centron and UNIQ...

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

Class II — Potential Health HazardOngoing