Reported Feb 7, 2018 · Terminated

YANSHIJIAONANG capsules, 2000mg, 8-count bottle, labeling is in foreign language

A&H Focal Inc.

High riskUsing this product could cause serious injury, illness or death — stop using it now.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: A&H Focal Inc. · 119 Linwood Ave · Staten Island, NY · 10305-4445

Is this the product you have?

  • YANSHIJIAONANG capsules, 2000mg, 8-count bottle, labeling is in foreign language
Lot codes and dates
  • All Lots
Amount recalled
unknown

This recall covers 21 products

The agency filed one notice per product. You are reading one of them; the other 20 are below.

8 more are in the archive.

Where it was sold

Why it was recalled

Stop using this product now

Marked Without An Approved NDA/ANDA: FDA analysis found these products to contain sildenafil, an FDA approved drug for the treatment of erectile dysfunction, making these products unapproved drugs for which safety and efficacy have not been establish and therefore, subject to recall.

Using this product could cause serious injury, illness or death — stop using it now.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA drug enforcement) notice

Notice updated Jun 14, 2019 · Data as of Sep 19, 7:17 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.