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 3668136700 of 51,434 recalls

FoodDecember 2, 2015· Jem Raw Chocolate, LLC

Recalled Item: Cashew Cardamom - Sprouted Cashew Almond Spread. Product is packaged...

The Issue: Cashew Cardamom - Sprouted Cashew Almond Spread is recalled because it has...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 2, 2015· Jem Raw Chocolate, LLC

Recalled Item: Superberry Maqui Camu - Sprouted Almond Spread. Product is packaged Recalled...

The Issue: Superberry Maqui Camu - Sprouted Almond Spread is recalled because it has...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 2, 2015· Pfizer Inc.

Recalled Item: Norpace CR (disopyramide phosphate) extended-release capsules USP Recalled...

The Issue: Failed Dissolution Specification

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

Class III — Low RiskOngoing
Refund
Medical DeviceDecember 1, 2015· Beckman Coulter Inc.

Recalled Item: UniCel DxH 800 Coulter Cellular Analysis System Recalled by Beckman Coulter...

The Issue: Beckman Coulter is recalling the DxH 800 Slidemaker Stainer Software version...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2015· Beckman Coulter Inc.

Recalled Item: MicroScan Pos Combo Panel Type 33 Recalled by Beckman Coulter Inc. Due to...

The Issue: Beckman Coulter has confirmed falsely negative results for Voges-Proskauer...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2015· Beckman Coulter Inc.

Recalled Item: MicroScan Pos Combo Panel Type 21 Recalled by Beckman Coulter Inc. Due to...

The Issue: Beckman Coulter has confirmed falsely negative results for Voges-Proskauer...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2015· Beckman Coulter Inc.

Recalled Item: MicroScan Pos Breakpoint Combo Panel Type 23 Recalled by Beckman Coulter...

The Issue: Beckman Coulter has confirmed falsely negative results for Voges-Proskauer...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2015· 3M Company - Health Care Business

Recalled Item: 3M Coban Self-Adherent Wrap Shipper carton label identified the product...

The Issue: Product mislabeled as latex free. Actual Catalog number 1581, lot 2020-10AN....

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2015· Beckman Coulter Inc.

Recalled Item: MicroScan Pos Combo Panel Type 34 Recalled by Beckman Coulter Inc. Due to...

The Issue: Beckman Coulter has confirmed falsely negative results for Voges-Proskauer...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2015· Draeger Medical, Inc.

Recalled Item: Optional PS500 Power Supply Unit for the Evita V500 Ventilator Recalled by...

The Issue: The firm became aware of cases in which the battery run times of the...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 1, 2015· Beckman Coulter Inc.

Recalled Item: UniCel DxH 600 Coulter Cellular Analysis System Recalled by Beckman Coulter...

The Issue: Beckman Coulter is recalling the DxH 800 Slidemaker Stainer Software version...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2015· Beckman Coulter Inc.

Recalled Item: UniCel DxH 600 Coulter Cellular Analysis System Recalled by Beckman Coulter...

The Issue: Beckman Coulter is recalling the DxH 800 Slidemaker Stainer Software version...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2015· Partners In Medicine Llc

Recalled Item: CNSystems TASK FORCE MONITOR 3040i Recalled by Partners In Medicine Llc Due...

The Issue: Device non-conformity which may lead to an incorrect oscillometric...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2015· Beckman Coulter Inc.

Recalled Item: MicroScan Pos Breakpoint Combo Panel Type 20 Recalled by Beckman Coulter...

The Issue: Beckman Coulter has confirmed falsely negative results for Voges-Proskauer...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2015· Synthes (USA) Products LLC

Recalled Item: SYNTHES Recalled by Synthes (USA) Products LLC Due to The 13.5mm Medullary...

The Issue: The 13.5mm Medullary Reamer head, lot #F-17180, is etched as dimension...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2015· JosNoe Medical, Inc.

Recalled Item: PS-500 Scope Warmer Recalled by JosNoe Medical, Inc. Due to Damage to...

The Issue: Damage to package seals potentially compromising sterility.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2015· Microbiologics Inc

Recalled Item: QC Sets and Panels: KWIK-STIK. Cepheid Xpert GBS QC Set Recalled by...

The Issue: The Lactobacillus acidophilus negative control (item 0243 single KWIK-STIK)...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 1, 2015· Microbiologics Inc

Recalled Item: QC Sets and Panels: KWIK-STIK Cepheid Smart GBS QC Set Recalled by...

The Issue: The Lactobacillus acidophilus negative control (item 0243 single KWIK-STIK)...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2015· Aesculap, Inc.

Recalled Item: Columbus Revision Knee System Recalled by Aesculap, Inc. Due to Aesculap...

The Issue: Aesculap Inc. US has initiated a recall on Tibial and Femur extension...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2015· Baxter Healthcare Corp.

Recalled Item: Baxter CLEARLINK System Recalled by Baxter Healthcare Corp. Due to Potential...

The Issue: Potential for dark loose particulate matter (400 microns or smaller) on the...

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

Class II — Potential Health HazardOngoing