Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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Class I · High risk Terminated Initiated Jun 27, 2013 (13 years ago)

Silver Sword capsules

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Marketed without an Approved NDA/ANDA: Laboratory analysis conducted by the FDA has determined that the products was found to contain sildenafil, an undeclared active pharmaceutical ingredient.

Cause type: Chemical / undeclared

A chemical that should not be there - benzene, methanol, lead - or an undeclared prescription drug hidden in a supplement. The label gives no warning: you may be taking a toxic solvent, a heavy metal, or a drug such as sildenafil that interacts with your other medicines. All chemical / undeclared recalls.

What was recalled

Silver Sword capsules, 180 mg, 16-count clamshell tin, UPC 1 234658 970128 12345 (labeling is in foreign language)

Recalling firm
Fabscout Entertainment, Inc
Origin
FL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1170-2014 · FDA notice

Treat this as urgent. Class I means FDA judged there is a reasonable probability of serious harm. Find the lot number on your package; if it matches the recalled lots, do not take another dose before you have spoken to your pharmacist or prescriber - today, not next week. This recall is now terminated, which means the firm has finished removing the affected product; anything on pharmacy shelves today should be unaffected.

Other recalls by Fabscout Entertainment, Inc

All 2013 recalls
Class I · High risk

Evil Root 1200 mg

Marketed without an Approved NDA/ANDA: product found to contain undeclared sildenafil

Terminated Chemical / undeclared Fabscout Entertainment, Inc D-376-2014
Class I · High risk

Clalis capsules

Marketed without an Approved NDA/ANDA: Laboratory analysis conducted by the FDA has determined that the products was found to contain sildenafil, an undeclared active pharmaceutical ingredient.

Terminated Chemical / undeclared Fabscout Entertainment, Inc D-1169-2014

Other chemical / undeclared recalls from 2013

All chemical / undeclared recalls
Class I · High risk

Burn 7 Capsules

Marketed Without an Approved NDA/ANDA: Undeclared sibutramine and phenolphthalein in Burn 7 dietary supplement

Terminated Chemical / undeclared Deseo Rebajar D-1351-2014
Class I · High risk

Dream Body Slimming Capsule

Marketed Without An Approved NDA/ANDA: The product contains undeclared sibutramine and . Sibutramine is not currently marketed in the United States, making this product an unapproved new drug.

Terminated Chemical / undeclared Slim Beauty USA D-1222-2014
Class I · High risk

Magic Slim capsules

Marketed Without An Approved NDA/ANDA: The product contains undeclared sibutramine and phenolphthalein. Marketed Without An Approved NDA/ANDA: The product contains undeclared sibutramine and phenolphthalein. Sibutramine and phenolphthalein are not currently marketed in the United States, making this product an unapproved new drug.

Terminated Chemical / undeclared Slim Beauty USA D-1221-2014
Class I · High risk

Dr. Ming's Chinese Capsule

Marketed Without An Approved NDA/ANDA: The product contains undeclared sibutramine and phenolphthalein. Sibutramine and phenolphthalein are not currently marketed in the United States, making this product an unapproved new drug.

Terminated Chemical / undeclared Slim Beauty USA D-1220-2014