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Class I · High risk Terminated Initiated Sep 27, 2013 (13 years ago)

PHUK Sexual Enhancement Ultimate Pleasure

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

Why it was recalled

Marketed without an Approved NDA/ANDA: Dietary supplement may contain amounts of active ingredients found in some FDA-approved drugs for erectile dysfunction (ED) making the dietary supplement an unapproved drug.

Cause type: Unapproved drug

The product was marketed without an approved NDA/ANDA, or does not meet the OTC monograph it claims to follow. Nothing about the product - dose, purity, safety - has been reviewed by FDA, so the claims on the box are unverified. All unapproved drug recalls.

What was recalled

PHUK Sexual Enhancement Ultimate Pleasure, 400mg/capsule, packaged in 1 and 2 capsule blister packs and 4,12,24 capsule bottles, Distributed by UME Supplements, INC www.phukherbal.com.

Recalling firm
Haute Health, LLC
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1236-2014 · 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 Haute Health, LLC

All 2013 recalls
Class I · High risk

Virilis Pro

Marketed without an Approved NDA/ANDA: Dietary supplement may contain amounts of active ingredients found in some FDA-approved drugs for erectile dysfunction (ED) making the dietary supplement an unapproved drug.

Terminated Unapproved drug Haute Health, LLC D-1237-2014
Class I · High risk

Prolifta Dietary Supplement Prolifta

Marketed without an Approved NDA/ANDA: Dietary supplement may contain amounts of an active ingredient found in some FDA-approved drugs for erectile dysfunction (ED) making the dietary supplement an unapproved drug.

Terminated Unapproved drug Haute Health, LLC D-1235-2014

Other unapproved drug recalls from 2013

All unapproved drug recalls
Class II · Moderate risk

HydrOXYzine HCI Tablets USP 50 mg

Good Manufacturing Practices Deviations: The product has an Active Pharmaceutical Ingredient from an unapproved source.

Terminated Unapproved drug KVK-Tech, Inc. D-1032-2014
Class II · Moderate risk

HydrOXYzine HCI Tablets USP 25 mg

Good Manufacturing Practices Deviations: The product has an Active Pharmaceutical Ingredient from an unapproved source.

Terminated Unapproved drug KVK-Tech, Inc. D-1031-2014
Class II · Moderate risk

HydrOXYzine HCI Tablets USP 10 mg

Good Manufacturing Practices Deviations: The product has an Active Pharmaceutical Ingredient from an unapproved source.

Terminated Unapproved drug KVK-Tech, Inc. NDC 10702-010-01 D-1030-2014
Class I · High risk

Virilis Pro

Marketed without an Approved NDA/ANDA: Dietary supplement may contain amounts of active ingredients found in some FDA-approved drugs for erectile dysfunction (ED) making the dietary supplement an unapproved drug.

Terminated Unapproved drug Haute Health, LLC D-1237-2014