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. 2,418 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
2,418 in last 12 months

Showing 4602146040 of 51,434 recalls

DrugSeptember 9, 2013· PACK Pharmaceuticals, LLC

Recalled Item: Timolol Maleate Sterile Ophthalmic Solution Recalled by PACK...

The Issue: Defective Container: Stability samples of both products were noted to have...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 9, 2013· PACK Pharmaceuticals, LLC

Recalled Item: Timolol Maleate Sterile Ophthalmic Solution Recalled by PACK...

The Issue: Defective Container: Stability samples of both products were noted to have...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 9, 2013· Avella of Deer Valley, Inc.

Recalled Item: Vancomycin PF (BSS) 1% Recalled by Avella of Deer Valley, Inc. Due to Lack...

The Issue: Lack of Assurance of Sterility: Avella Specialty Pharmacy is recalling...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 9, 2013· Avella of Deer Valley, Inc.

Recalled Item: Bevacizumab 1.25 mg/0.05 mL PF Recalled by Avella of Deer Valley, Inc. Due...

The Issue: Lack of Assurance of Sterility: Avella Specialty Pharmacy is recalling...

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 9, 2013· Pharmavite Corporation

Recalled Item: Multi for Her 50+ (Full Strength Mini and Multi softgels) Recalled by...

The Issue: Pharmavite LLC is conducting a voluntary recall of all lots of its Nature...

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 9, 2013· Pharmavite Corporation

Recalled Item: Multi for Her (Full Strength Mini and Multi Softgels) Recalled by Pharmavite...

The Issue: Pharmavite LLC is conducting a voluntary recall of all lots of its Nature...

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 9, 2013· Pharmavite Corporation

Recalled Item: Multi For Him (Full Strength Mini and Multi Softgels) Recalled by Pharmavite...

The Issue: Pharmavite LLC is conducting a voluntary recall of all lots of its Nature...

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 9, 2013· Pharmavite Corporation

Recalled Item: Multi Complete (Full Strength Mini and Multi Softgels) Recalled by...

The Issue: Pharmavite LLC is conducting a voluntary recall of all lots of its Nature...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 9, 2013· Hospira Inc.

Recalled Item: *** 1) Product labeled in part: 14951-48 Recalled by Hospira Inc. Due to...

The Issue: Intravenous fluid may leak at the CLAVE secondary port of Hospira PlumSet IV...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2013· Hospira Inc.

Recalled Item: *** 1) Product labeled in part: List No. 14220-28 Recalled by Hospira Inc....

The Issue: Intravenous fluid may leak at the CLAVE secondary port of Hospira PlumSet IV...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2013· Hospira Inc.

Recalled Item: *** 1) Product labeled in part: 19734-28 Recalled by Hospira Inc. Due to...

The Issue: Intravenous fluid may leak at the CLAVE secondary port of Hospira PlumSet IV...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2013· Hospira Inc.

Recalled Item: *** 1) Product labeled in part: 19683-28 Recalled by Hospira Inc. Due to...

The Issue: Intravenous fluid may leak at the CLAVE secondary port of Hospira PlumSet IV...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2013· Hospira Inc.

Recalled Item: *** 1) Product labeled in part: List No. 14212-28 Recalled by Hospira Inc....

The Issue: Intravenous fluid may leak at the CLAVE secondary port of Hospira PlumSet IV...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2013· Beckman Coulter Inc.

Recalled Item: ISE Recalled by Beckman Coulter Inc. Due to The recall was initiated because...

The Issue: The recall was initiated because Beckman Coulter has confirmed that some AU...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2013· Beckman Coulter Inc.

Recalled Item: ISE Recalled by Beckman Coulter Inc. Due to The recall was initiated because...

The Issue: The recall was initiated because Beckman Coulter has confirmed that some AU...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 9, 2013· Becton Dickinson & Co.

Recalled Item: BBL (tm) MGIT (tm) Mycobacteria Growth Indicator Tube Recalled by Becton...

The Issue: An in-vitro diagnostic reagent may be labeled with an incorrect barcode,...

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

Class II — Potential Health HazardOngoing
DrugSeptember 8, 2013· Hill Dermaceuticals, Inc.

Recalled Item: Derma-Smoothe/FS (fluocinolone acetonide) 0.01% Topical Oil (Body Oil)...

The Issue: Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 8, 2013· Hill Dermaceuticals, Inc.

Recalled Item: Derma-Smoothe/FS (fluocinolone acetonide) 0.01% Topical Oil (Scalp Oil)...

The Issue: Subpotent Drug: The active ingredient, fluocinolone acetonide, was found to...

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

Class III — Low RiskOngoing
Refund
FoodSeptember 7, 2013· Semifreddi's Inc.

Recalled Item: Almond Biscotti Recalled by Semifreddi's Inc. Due to Undeclared Allergens

The Issue: Semifreddi's Almond Biscotti and Semifreddi's Chocolate Dipped Almond...

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 7, 2013· Semifreddi's Inc.

Recalled Item: Chocolate Dipped Almond Biscotti Recalled by Semifreddi's Inc. Due to...

The Issue: Semifreddi's Almond Biscotti and Semifreddi's Chocolate Dipped Almond...

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

Class II — Potential Health HazardOngoing
Refund