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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 66043

3 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
August 14, 2013
Product types
Drug
Classifications
Class I
Statuses
Terminated
Recalling firm wording
Fabscout Entertainment, Inc

Dossier provenance

Source snapshots represented here

  • openFDA Drug Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

3 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

drug · product 1 of 3

Evil Root 1200 mg, supplied in 6 capsules per bottle, Manufacturer: Tibet Shengyang Health Medicine Co.,Ltd. Address: No. 98, Min zu Road, Lhasa

D-376-2014
Recall number
D-376-2014
Initiated
August 14, 2013
Classification
Class I
Status
Terminated
Quantity
32 bottles of 6 capsules each

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Marketed without an Approved NDA/ANDA: product found to contain undeclared sildenafil

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

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

Code information

All Lots

Distribution pattern

CA, FL and UT

drug · product 2 of 3

72HP MAXIMUM POTENCY MALE SEXUAL ENHANCEMENT, Dietary Supplement, supplied in 1 capsule per blister pack, Distributed by: 72HP, Inc. Weston, FL

D-377-2014
Recall number
D-377-2014
Initiated
August 14, 2013
Classification
Class I
Status
Terminated
Quantity
578 blister packs of 1 capsule each

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Marketed without an Approved NDA/ANDA: products were found to contain undeclared sildenafil

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

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

Code information

All Lots

Distribution pattern

CA, FL and UT

drug · product 3 of 3

PRO POWER MAX Natural Energy Enhancer, ALL NATURAL HERBS, supplied in 1 capsule per blister pack, Distributed by MSH Distribution LLC

D-378-2014
Recall number
D-378-2014
Initiated
August 14, 2013
Classification
Class I
Status
Terminated
Quantity
18 blister packs of one capsule each

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Marketed without an Approved NDA/ANDA: product found to contain undeclared sildenafil and tadalafil

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

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

Code information

All Lots

Distribution pattern

CA, FL and UT