Fresh Recalls

FDAClass II · Drug · Recall D-0759-2026 · Recalled August 19, 2026

SILDENAFIL CITRATE USP recall — Shoolin Pharma Chem LLP

Agency report date: August 19, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
SILDENAFIL CITRATE USP
Company / brand
Shoolin Pharma Chem LLP
Lot / serial / date codes
Batch SDC2505001, Date of Expiry: April 30, 2030.
Distribution
Distributed Nationwide in the USA
Agency product description and boundaries

SILDENAFIL CITRATE USP, 0.100 KG, 100 gm-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, Mahesana, Gujarat, 382715, India, (CAS NO. 171599-83-0) NDC 85702-001-05

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: CGMP Deviations:Noted during FDA inspection

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class II: may cause temporary or medically reversible health consequences.

Affected product: SILDENAFIL CITRATE USP

3. Open the official notice or contact

Official recall ID
D-0759-2026
Brand
Shoolin Pharma Chem LLP
Classification
Class II
Units affected
25KG, 250-1gm bags
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Kadi, India
Firm address
408 B/H Ratnamani Tubes, Block/Survey No; Nr Maruti Inox, N/A

Identifying details (verbatim from the notice)

Product codes / lots
Batch SDC2505001, Date of Expiry: April 30, 2030.
Distribution
Distributed Nationwide in the USA
FDA event ID
99547
Recall initiated
August 3, 2026
FDA classified
August 13, 2026
FDA report date
August 19, 2026
Verify with the official sources:

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked September 7, 2026 at 6:00 AM UTC. Record retrieved September 7, 2026 at 6:00 AM UTC.

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