US Drug Recall Register
Class II · Moderate risk Ongoing Initiated Aug 3, 2026 (30 days ago)

SILDENAFIL CITRATE USP, 1.00KG, 1.00KG-bag Net Wt. Rx only " For Prescription Compounding…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

CGMP Deviations:Noted during FDA inspection

What was recalled

SILDENAFIL CITRATE USP, 1.00KG, 1.00KG-bag Net Wt. Rx only " For Prescription Compounding Only", Shoolin Pharma Chem LLP, Block/Survey no 408, B/H Ratnamani Tubes, Near Maruti Inox, Indrad, Kadi, Mahesania, Gujarat, 382715, India, (CAS NO. 171599-83-0) NDC 85702-001-08.

Recalling firm
Shoolin Pharma Chem LLP
NDC code
85702-001-08
Origin
India
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0763-2026

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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Reason Labeling: Incorrect or missing lot and/or expiration date. Products were compounded using expired components.

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Reason Labeling: Incorrect or missing lot and/or expiration date. Products were compounded using expired components.

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