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. 1,015 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
1,015 in last 12 months

Showing 34841–34860 of 51,434 recalls

FoodMay 2, 2016· CRF Frozen Foods, LLC

Recalled Item: Supreme Stir-Fry Sensation Recalled by CRF Frozen Foods, LLC Due to...

The Issue: Supreme Stir-Fry Sensation is recalled because it has the potential to be...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 2, 2016· CRF Frozen Foods, LLC

Recalled Item: Organic Steamers Roasted Red Potato & Vegetable Medley Recalled by CRF...

The Issue: Potoatoes, Beans, Peppers, and Mushrooms mixes are recalled because they...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 2, 2016· CRF Frozen Foods, LLC

Recalled Item: Organic Peas & Pearl Onions Recalled by CRF Frozen Foods, LLC Due to...

The Issue: Organic Peas & Pearl Onions are recalled because they have the potential to...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 2, 2016· CRF Frozen Foods, LLC

Recalled Item: Organic Peaches Recalled by CRF Frozen Foods, LLC Due to Potential Listeria...

The Issue: Organic Peaches are recalled because they have the potential to be...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 2, 2016· CRF Frozen Foods, LLC

Recalled Item: Organic Butternut Squash Recalled by CRF Frozen Foods, LLC Due to Potential...

The Issue: Butternut Squash are recalled because they have the potential to be...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 2, 2016· SunOpta Food and Grain, Inc.

Recalled Item: 1. Roasted Not Salted Sunflower Kernel Recalled by SunOpta Food and Grain,...

The Issue: SunOpta is recalling sunflower kernel products that have the potential to be...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 2, 2016· Sandoz, Inc

Recalled Item: Dicloxacillin Sodium Capsules Recalled by Sandoz, Inc Due to Failed...

The Issue: Failed Impurities/Degradation Specifications:Out of specification result for...

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

Class III — Low RiskOngoing
Refund
DrugMay 2, 2016· Sandoz, Inc

Recalled Item: Dicloxacillin Sodium Capsules USP Recalled by Sandoz, Inc Due to Failed...

The Issue: Failed Impurities/Degradation Specifications:Out of specification result for...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMay 2, 2016· Leica Biosystems Richmond Inc.

Recalled Item: CytoVision Image Analysis and Capture System Recalled by Leica Biosystems...

The Issue: Systems have an improperly activated Windows 7 OS, even though a valid...

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

Class III — Low RiskOngoing
Medical DeviceMay 2, 2016· Siemens Healthcare Diagnostics, Inc

Recalled Item: Siemens Healthcare ADVIA Centaur Tnl-Ultra Assay . In-Vitro Diagnostic for...

The Issue: Exhibits a greater than 10% change in results in samples with biotin levels...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2016· Synthes (USA) Products LLC

Recalled Item: 1.5 mm Rapid Resorb Orbt1 F1 P1 w/Bending Template / 24 mm - Sterile...

The Issue: Labeling errors. The outer packge label expiration date may exceed the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2016· Synthes (USA) Products LLC

Recalled Item: DePuy Synthes 8.0 mm Flexible Shaft Reamer Recalled by Synthes (USA)...

The Issue: Devices did not pass the biological safety evaluation for cytotoxicity...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2016· Synthes (USA) Products LLC

Recalled Item: 1.5 mm Rapid Resorb Orbt1 F1 P1 w/Bending Template / 35 mm - Sterile...

The Issue: Labeling errors. The outer packge label expiration date may exceed the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 2, 2016· Synthes (USA) Products LLC

Recalled Item: 1.5 mm Rapid Resorb Orbt1 F1 P1 w/Bending Template / 30 mm - Sterile...

The Issue: Labeling errors. The outer packge label expiration date may exceed the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core128 Model No. 728323 Recalled by Philips Medical Systems...

The Issue: Software issues in v4.1.3/4.1.4/4.1.5 in the Philips Ingenuity CT products...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 64 CT Model 728231 Recalled by Philips Medical Systems...

The Issue: Software issues found in software versions v4.1.3/4.1.4/4.1.5 in the Philips...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance iCT SP Model No. 728311 Recalled by Philips Medical Systems...

The Issue: Software issues found in v4.1 .3/4.1.5 in the Philips Brilliance iCT/ iCT SP...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity CT Model No. 728326 Recalled by Philips Medical Systems...

The Issue: Software issues in v4.1.3/4.1.4/4.1.5 in the Philips Ingenuity CT products...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core Model No. 728321 Recalled by Philips Medical Systems...

The Issue: Software issues in software versions v4.1.3/4.1.4/4.1.5 in the Philips...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 29, 2016· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance iCT Recalled by Philips Medical Systems (Cleveland) Inc Due to...

The Issue: Software issues in versions v4.1 .3/4.1.5 in the Philips Brilliance iCT) iCT...

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

Class II — Potential Health HazardOngoing