Recall archive / FDA drug enforcement

TRI-MIX PAPAVERINE 15/PHENTOLAMINE 0.5/PGE-1 5 INJ INJECTABLE, Rx only, Talon Compounding Pharmacy, 2950 Thousand Oak... — FDA record D-0187-2022

Reported terminated

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Oct 12, 2021. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.

What the record says

Product: TRI-MIX PAPAVERINE 15/PHENTOLAMINE 0.5/PGE-1 5 INJ INJECTABLE, Rx only, Talon Compounding Pharmacy, 2950 Thousand Oaks Drive Ste 25, San Antonio, Texas 78247
Reason: Lack of assurance of sterility
Classification: Class II
Recalling firm: Vita Pharmacy, LLC dba Talon Compounding Pharmacy
Quantity: 2 vials
Agency-reported status: Terminated
Source record identifier: D-0187-2022

Open the official record

What the recall classes mean. Classification is an agency assessment, not individual medical advice.

Lot and product identifiers

Label field	Details supplied by the agency
Lot, code or applicability	Lot: 07292021:21 BUD: 11/30/2021

Match all identifying details in the current notice. A brand name alone is not enough.

Distribution

United States including Washington, D.C. and Puerto Rico

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

Washington

Dates in the source

Report date: Nov 17, 2021
Recall initiation date: Oct 12, 2021
Center classification date: Nov 8, 2021
Termination date: Oct 4, 2023

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.