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. 999 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
999 in last 12 months

Showing 37841–37860 of 51,434 recalls

DrugAugust 24, 2015· Novacare, LLC

Recalled Item: Asia Black 25 Ephedra Extreme Fat Burner Potent Dietary Supplement Recalled...

The Issue: Marketed Without an Approved NDA/ANDA: FDA sampling confirmed the presence...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 24, 2015· Novacare, LLC

Recalled Item: Thin and Slim Burn Fat Now Dietary Supplement packaged in Recalled by...

The Issue: Marketed Without an Approved NDA/ANDA: FDA sampling confirmed the presence...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 24, 2015· Novacare, LLC

Recalled Item: Black Widow 25 Ephedra Super Potent Fat Burner Dietary Supplement Recalled...

The Issue: Marketed Without an Approved NDA/ANDA: FDA sampling confirmed the presence...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 24, 2015· Novacare, LLC

Recalled Item: Xcellerator (product not labeled) Recalled by Novacare, LLC Due to Marketed...

The Issue: Marketed Without an Approved NDA/ANDA: FDA sampling confirmed the presence...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 24, 2015· Allergan Sales, LLC

Recalled Item: P.M. (Mineral Oil 42.5% and White Petrolatum 57.3%) Lubricant Recalled by...

The Issue: Presence of Particulate Matter: Due to customer complaints of small black...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 24, 2015· Allergan Sales, LLC

Recalled Item: BLEPHAMIDE (sulfacetamide sodium and prednisolone acetate ophthalmic...

The Issue: Presence of Particulate Matter: Due to customer complaints of small black...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 24, 2015· Novacare, LLC

Recalled Item: TruTrim (product not labeled) Recalled by Novacare, LLC Due to Marketed...

The Issue: Marketed Without an Approved NDA/ANDA: FDA sampling confirmed the presence...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 24, 2015· Allergan Sales, LLC

Recalled Item: FML (fluorometholone ophthalmic ointment) 0.1% Recalled by Allergan Sales,...

The Issue: Presence of Particulate Matter: Due to customer complaints of small black...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 24, 2015· Allergan Sales, LLC

Recalled Item: Lacri-Lube (Mineral Oil 42.5% and White Petrolatum 56.8%) Lubricant Recalled...

The Issue: Presence of Particulate Matter: Due to customer complaints of small black...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 24, 2015· Novacare, LLC

Recalled Item: Thin and Slim MaxOut Body Max Out FX Fat Burner Recalled by Novacare, LLC...

The Issue: Marketed Without an Approved NDA/ANDA: FDA sampling confirmed the presence...

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 24, 2015· Novacare, LLC

Recalled Item: The Store Thin and Slim Thermogenic Fat Burner Dietary Supplement Recalled...

The Issue: Marketed Without an Approved NDA/ANDA: FDA sampling confirmed the presence...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceAugust 24, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens RAPIDPoint 500 Measurement Cartridge Lactate (100) tests Part...

The Issue: RAPIDPoint 500 measurement cartridge serial numbers 2517102517 through...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens RAPIDPoint 500 Measurement Cartridge Lactate (750 tests) Part...

The Issue: RAPIDPoint 500 measurement cartridge serial numbers 2517102517 through...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· Terumo Cardiovascular Systems Corp

Recalled Item: Terumo Custom Cardiovascular Procedure Kit X-Coated PED/Adult Main Pack P/N:...

The Issue: Custom Cardiovascular Procedure Kits contain recalled component Medivators...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· Siemens Healthcare Diagnostics Inc

Recalled Item: Siemens RAPIDPoint 500 Measurement Cartridge Lactate (400) tests Part...

The Issue: RAPIDPoint 500 measurement cartridge serial numbers 2517102517 through...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· Terumo Cardiovascular Systems Corp

Recalled Item: Terumo Custom Cardiovascular Procedure Kit Tubing Pack P/N: 66041-1 Terumo...

The Issue: Custom Cardiovascular Procedure Kits contain recalled component Medivators...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· Terumo Cardiovascular Systems Corp

Recalled Item: Terumo Custom Cardiovascular Procedure Kit X-Coated Perfusion Pack with...

The Issue: Custom Cardiovascular Procedure Kits contain recalled component Medivators...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· Terumo Cardiovascular Systems Corp

Recalled Item: Terumo Custom Cardiovascular Procedure Kit X-Coated PED/Adult Main Pack P/N:...

The Issue: Custom Cardiovascular Procedure Kits contain recalled component Medivators...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· STERILMED, INC.

Recalled Item: Zimmer Recalled by STERILMED, INC. Due to Mislabeling

The Issue: Sterilmed, Inc. is recalling its reprocessed Zimmer Tourniquet Cuff, Part...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2015· Terumo Cardiovascular Systems Corp

Recalled Item: Terumo Custom Cardiovascular Procedure Kit X-Coated Adult Pak P/N: 73124...

The Issue: Custom Cardiovascular Procedure Kits contain recalled component Medivators...

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

Class II — Potential Health HazardOngoing