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 3650136520 of 51,434 recalls

DrugDecember 17, 2015· Virtus Pharmaceuticals, Llc

Recalled Item: VP-CH-PNV PRENATAL/POSTNATAL Prescription Folic Acid-Containing Dietary...

The Issue: Defective Delivery System: Product may contain leaking capsules.

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

Class III — Low RiskOngoing
Refund
FoodDecember 17, 2015· Mars Chocolate North America

Recalled Item: Dove Chocolate Assortment Snowflakes Net. Wt. 24.0 oz. Distributed by...

The Issue: Dove Chocolate Assortment Snowflakes may contain undeclared peanuts, what...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 16, 2015· Twinings North America, Inc.

Recalled Item: TWININGS OF London ENGLISH BREAKFAST BLACK TEA DECAFFEINATED Recalled by...

The Issue: Twinings English Breakfast Black Tea 12ct Kcups, were packaged in cartons...

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

Class III — Low RiskOngoing
Refund
Medical DeviceDecember 16, 2015· Maquet Datascope Corp - Cardiac Assist Division

Recalled Item: Cardiosave Hybrid and rescue IABP Recalled by Maquet Datascope Corp -...

The Issue: Maquet has recieved information that in some Cardiosave IABPS, the scroll...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2015· Stryker Spine

Recalled Item: AccuLIF PL Tubing Set and AccuLIF TL Tubing Set AccuLIF Recalled by Stryker...

The Issue: There were two potential interference conditions identified with the way the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2015· GE Inspection Technologies, LP

Recalled Item: GE Inspection Technologies Recalled by GE Inspection Technologies, LP Due to...

The Issue: GE Inspection Technologies, LP ("GE") has discovered that certain of its...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2015· GE Medical Systems, LLC

Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to The Drive Gas Check...

The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2015· GE Medical Systems, LLC

Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to The Drive Gas Check...

The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2015· GE Medical Systems, LLC

Recalled Item: Anesthesia device service kits. ASSY-MSN Recalled by GE Medical Systems, LLC...

The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2015· GE Medical Systems, LLC

Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to The Drive Gas Check...

The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2015· GE Medical Systems, LLC

Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to The Drive Gas Check...

The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2015· GE Medical Systems, LLC

Recalled Item: GE Healthcare Recalled by GE Medical Systems, LLC Due to The Drive Gas Check...

The Issue: The Drive Gas Check Valve of certain Anesthesia products could become stuck...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2015· Mindray DS USA, Inc. dba Mindray North America

Recalled Item: Panorama Patient Monitoring Network. Software Kit 0020-00-0205-19A Recalled...

The Issue: An issue with the Panorama Central Station may cause the system to...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2015· Fresenius Medical Care Renal Therapies Group, LLC

Recalled Item: Fresenius Liberty Cycler-Peritoneal Dialysis Cycler Model: 180111 and...

The Issue: The door latch may not fully close and the door may open unexpectedly. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2015· Globalmed Logistix

Recalled Item: Lipogems SPA Aspiration Cannulae Recalled by Globalmed Logistix Due to The...

The Issue: The cannulae may bend during procedure.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2015· Bio-Rad Laboratories, Inc.

Recalled Item: D-10 Rack Loader Recalled by Bio-Rad Laboratories, Inc. Due to On a rare...

The Issue: On a rare occasion, there is a potential to assign a patient result to an...

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

Class II — Potential Health HazardOngoing
FoodDecember 15, 2015· Trader Joes Company

Recalled Item: Triple Ginger Brew Recalled by Trader Joes Company Due to Trader Joes...

The Issue: Trader Joes recalling Triple Ginger Brew due to reports of unopened bottles...

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

Class III — Low RiskOngoing
Refund
DrugDecember 15, 2015· Bee Extremely Amazed LLC

Recalled Item: SLIM TRIM U Capsules Recalled by Bee Extremely Amazed LLC Due to Undeclared...

The Issue: Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 15, 2015· Morton Grove Pharmaceuticals, Inc.

Recalled Item: Lindane Lotion Recalled by Morton Grove Pharmaceuticals, Inc. Due to...

The Issue: Super-Potent Drug: Out of Specification Assay test results were reported for...

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

Class III — Low RiskOngoing
Refund
DrugDecember 15, 2015· Bee Extremely Amazed LLC

Recalled Item: SlimeX-15 Capsules Recalled by Bee Extremely Amazed LLC Due to Undeclared...

The Issue: Marketed Without An Approved NDA/ANDA: tainted product marketed as a dietary...

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

Class I — Serious Health HazardOngoing
Refund