Recall events
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Event 68218
Event summary
Timeline bucket May 05, 2014
Product types Drug
Classifications Class I
Statuses Terminated
Recalling firm wording Eugene Oregon, 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
Black Ant, 2800 mg, four capsules per box, Manufacturer Qinghai Baojiantang Pharmaceutical Co., Ltd.
D-1613-2014
Recall number D-1613-2014
Initiated May 05, 2014
Classification Class I
Status Terminated
Quantity 136 boxes
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Marketed Without an Approved NDA/ANDA: Eugene FDA laboratory analyses determined they 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: Eugene FDA laboratory analyses determined they contain undeclared sildenafil.
Distribution pattern To retailers in MD, TX, FL, PA, IL, NJ, IN, LA, WA, ME, SC
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[6162]
FDA event record
· Exact recall-number query on openFDA
drug · product 2 of 3
MOJO RISEN, 650 mg, 2 capsule per pouch, Distributed by: Mojo Risen, LLC, Springville, UT 84663
D-1614-2014
Recall number D-1614-2014
Initiated May 05, 2014
Classification Class I
Status Terminated
Quantity 57 boxes
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Marketed Without an Approved NDA/ANDA: Eugene FDA laboratory analyses determined they 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: Eugene FDA laboratory analyses determined they contain undeclared sildenafil.
Distribution pattern To retailers in MD, TX, FL, PA, IL, NJ, IN, LA, WA, ME, SC
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[5770]
FDA event record
· Exact recall-number query on openFDA
drug · product 3 of 3
AFRICAN BLACK ANT, 2800 mg, 6 capsules per box, produced by: Qinghan Hongwei Bioengineering Company, No. 158, Renmin Road, Xining City.
D1612-2014
Recall number D1612-2014
Initiated May 05, 2014
Classification Class I
Status Terminated
Quantity 460 boxes
App-derived interpretation
Unknown
reason.no_named_rule · v1.0.0
Marketed Without an Approved NDA/ANDA: Eugene FDA laboratory analyses determined they 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: Eugene FDA laboratory analyses determined they contain undeclared sildenafil.
Distribution pattern To retailers in MD, TX, FL, PA, IL, NJ, IN, LA, WA, ME, SC
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[7652]
FDA event record
· Exact recall-number query on openFDA
