Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Alprostadil Container Description: Amber color bottle Recalled by Aspen Biopharma Labs Pvt., Ltd. Due to CGMP Deviations
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Aspen Biopharma Labs Pvt., Ltd. directly.
Affected Products
Alprostadil Container Description: Amber color bottle
Quantity: 3.0 gm
Why Was This Recalled?
CGMP Deviations
Where Was This Sold?
Product was distributed to 3 distributors (1 Hong Kong and 2 accounts in Florida)
About Aspen Biopharma Labs Pvt., Ltd.
Aspen Biopharma Labs Pvt., Ltd. has 6 total recalls tracked by RecallDetector.
Related Recalls
Icosapent Ethyl Capsules Recalled by Zydus Pharmaceuticals (USA) Inc Due to Failed Tablet/Capsule specifications: Red dots inside capsule and...
Zydus Pharmaceuticals (USA) Inc · March 9, 2026
Product label: Temozolomide Capsules Recalled by Rising Pharma Holding, Inc. Due to Failed Impurities/Degradation Specifications: An out-of-specification result observed during...
Rising Pharma Holding, Inc. · March 3, 2026
Semaglutide Inj. Recalled by New Life Pharma LLC Due to Lack of Assurance of Sterility
New Life Pharma LLC · February 26, 2026
Tirzepatide Inj Recalled by New Life Pharma LLC Due to Lack of Assurance of Sterility
New Life Pharma LLC · February 26, 2026
Tirzepatide Inj Recalled by New Life Pharma LLC Due to Lack of Assurance of Sterility
New Life Pharma LLC · February 26, 2026
Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report