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. 2,724 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
2,724 in last 12 months

Showing 561580 of 13,494 recalls

DrugApril 28, 2025· BSO LLC

Recalled Item: TESTOSTERONE PELLET 200 mg BLUNT (with Cholesterol </=2%) Recalled by BSO...

The Issue: Presence of Particulate Matter: Glass particles were found in pellet vials.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 28, 2025· BSO LLC

Recalled Item: TESTOSTERONE PELLET 200 mg (with Cholesterol </=2%) Recalled by BSO LLC Due...

The Issue: Presence of Particulate Matter: Glass particles were found in pellet vials.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 23, 2025· BRS Analytical Services, LLC

Recalled Item: Artificial Tears Ophthalmic Solution Recalled by BRS Analytical Services,...

The Issue: cGMP deviations and lack of assurance of sterility.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 23, 2025· BRS Analytical Services, LLC

Recalled Item: Carboxymethylcellulose Sodium Ophthalmic Gel 1% Recalled by BRS Analytical...

The Issue: cGMP deviations and lack of assurance of sterility.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 23, 2025· BRS Analytical Services, LLC

Recalled Item: Polyvinyl Alcohol Ophthalmic Solution 1.4% Recalled by BRS Analytical...

The Issue: cGMP deviations and lack of assurance of sterility.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 23, 2025· BRS Analytical Services, LLC

Recalled Item: Lubricant Eye Drops Solution Recalled by BRS Analytical Services, LLC Due to...

The Issue: cGMP deviations and lack of assurance of sterility.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 23, 2025· BRS Analytical Services, LLC

Recalled Item: Carboxymethylcellulose Sodium Ophthalmic Solution 0.5% Recalled by BRS...

The Issue: cGMP deviations and lack of assurance of sterility.

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 21, 2025· Eugia US LLC

Recalled Item: Tirofiban Hydrochloride Injection 12.5 mg/250 mL (50 mcg/mL) Recalled by...

The Issue: Out-of-Specification test results were obtained in at long term conditions...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 21, 2025· Eugia US LLC

Recalled Item: Tirofiban Hydrochloride Injection 5 mg/100 mL (50 mcg/mL) Recalled by Eugia...

The Issue: Out-of-Specification test results were obtained in at long term conditions...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 18, 2025· FDC Limited

Recalled Item: Timolol Maleate Ophthalmic Solution USP Recalled by FDC Limited Due to...

The Issue: Defective Container: Unable to get the solution out of the bottle as the...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 18, 2025· American Regent, Inc.

Recalled Item: niCARdipine Hydrochloride Injection Recalled by American Regent, Inc. Due to...

The Issue: Lack of sterility assurance: Product leakage around the vial neck, which...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 18, 2025· American Regent, Inc.

Recalled Item: niCARdipine Hydrochloride Injection Recalled by American Regent, Inc. Due to...

The Issue: Lack of sterility assurance: Product leakage around the vial neck, which...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 18, 2025· Preferred Pharmaceuticals, Inc.

Recalled Item: Clindamycin Hydrochloride Capsules Recalled by Preferred Pharmaceuticals,...

The Issue: cGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 17, 2025· Amneal Pharmaceuticals, LLC

Recalled Item: Ropivacaine Hydrochloride Injection Recalled by Amneal Pharmaceuticals, LLC...

The Issue: Presence of Particulate Matter

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 15, 2025· OurPharma LLC

Recalled Item: HYDROmorphone Hydrochloride 50mg/50mL (1mg/mL) Recalled by OurPharma LLC Due...

The Issue: Superpotent Drug: Assay/potency result for hydromorphone HCl in the...

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

Class III — Low RiskOngoing
Refund
DrugApril 14, 2025· SAINI TRADE INC

Recalled Item: ELECTRO BUZZ Recalled by SAINI TRADE INC Due to Undeclared Chloropretadalafil

The Issue: Marketed without an Approved NDA/ANDA: Laboratory analysis found the product...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 14, 2025· SAINI TRADE INC

Recalled Item: ULTRA ARMOR Recalled by SAINI TRADE INC Due to Undeclared...

The Issue: Marketed without an Approved NDA/ANDA: Laboratory analysis found the product...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 14, 2025· SAINI TRADE INC

Recalled Item: Male Ultra Pro Recalled by SAINI TRADE INC Due to Undeclared...

The Issue: Marketed without an Approved NDA/ANDA: Laboratory analysis found the product...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 14, 2025· SAINI TRADE INC

Recalled Item: MALEXTRA Recalled by SAINI TRADE INC Due to Undeclared Propoxyphenylsildenafil

The Issue: Marketed without an Approved NDA/ANDA: Laboratory analysis found the product...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 14, 2025· SAINI TRADE INC

Recalled Item: Male Ultra Recalled by SAINI TRADE INC Due to Undeclared Propoxyphenylsildenafil

The Issue: Marketed without an Approved NDA/ANDA: Laboratory analysis found the product...

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

Class I — Serious Health HazardOngoing
Refund