Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Prostaglandin Tri-Mix 20:25:1 Injection Recalled by Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy Due to Lack of sterility assurance.
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 Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy directly.
Affected Products
Prostaglandin Tri-Mix 20:25:1 Injection, 2 mL Vial, Anderson Compounding Pharmacy 310 Bluff City Hwy, Bristol, TN.
Quantity: N/A
Why Was This Recalled?
Lack of sterility assurance.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy
Anderson Compounding Pharmacy, Inc. DBA Anderson Compounding Pharmacy has 68 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