RecallHawk
Class II Recall

SILDENAFIL CITRATE USP, 1.00KG, 1.00KG-bag Net Wt. Rx only " For Prescription Compounding Only", Shoolin Pharma Chem LL

Shoolin Pharma Chem LLP

Summary

The FDA issued a Class II for SILDENAFIL CITRATE USP, 1.00KG, 1.00KG-bag Net Wt. Rx only " For Prescription Co by Shoolin Pharma Chem LLP. Reason: CGMP Deviations:Noted during FDA inspection.

Details

Source

Drug Recall

External ID

D-0763-2026

Action Date

2026-08-19

Status

Ongoing

Category

drug

Product Description

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.

Lot/Code Info: Lot: SDC2505001, Date of Expiry: April 30, 2030.

Quantity Affected: 25 KG, 25 X 1.00 KG bags

Reason for Recall

CGMP Deviations:Noted during FDA inspection

Distribution

Distributed Nationwide in the USA

Type: Voluntary: Firm initiated

Recall Initiated: 2026-08-03

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 28 drug recalls issued in the same week, part of 68 drug-related FDA actions this month.

Shoolin Pharma Chem LLP has 5 FDA actions in our database, including 5 recalls.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Shoolin Pharma Chem LLP) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Shoolin Pharma Chem LLP have FDA actions?

Shoolin Pharma Chem LLP has 5 FDA actions in our database, including 5 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "D-0763-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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