Recall events
/
Event 66043
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
Device root-cause evidence is not applicable to this event.
No grouped product has the official product type device; this is not an unavailable-enrichment finding.
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
Distribution pattern CA, FL and UT
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[6311]
FDA event record
· Exact recall-number query on openFDA
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
Distribution pattern CA, FL and UT
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[5677]
FDA event record
· Exact recall-number query on openFDA
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
Distribution pattern CA, FL and UT
Official fact provenance
Dataset openFDA Drug Enforcement
Snapshot published July 16, 2026 07:03
Snapshot SHA-256 b791303a96cde04f35218bb062dc99bbd2aaedb7873ee857564b5dbe373c2651
Raw source locator 0001-drug-enforcement-0001-of-0001.json.zip#results[8610]
FDA event record
· Exact recall-number query on openFDA
