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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 65383

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

Open FDA event record

Event summary

Timeline bucket
May 20, 2013
Product types
Drug
Classifications
Class I
Statuses
Terminated
Recalling firm wording
Dolphin Intertrade Corporation

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

2 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 2

JaDera, 100% Natural Weight Loss Supplement, capsules, 30 count bottle

D-1249-2014
Recall number
D-1249-2014
Initiated
May 20, 2013
Classification
Class I
Status
Terminated
Quantity
998 boxes

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Marketed without an Approved NDA/ANDA: Products found to contain undeclared sibutramine. Sibutramine was removed from the U.S. market for safety reasons, making these products unapproved new drugs.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Marketed without an Approved NDA/ANDA: Products found to contain undeclared sibutramine. Sibutramine was removed from the U.S. market for safety reasons, making these products unapproved new drugs.

Code information

Manufacturing Codes: 10.06.2011 Exp. 09.06.2013

Distribution pattern

Nationwide

drug · product 2 of 2

XIYOUJI QINGZHI CAPSULE, 300mg, 20 count box

D-1250-2014
Recall number
D-1250-2014
Initiated
May 20, 2013
Classification
Class I
Status
Terminated
Quantity
8 bottles

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Marketed without an Approved NDA/ANDA: Products found to contain undeclared sibutramine. Sibutramine was removed from the U.S. market for safety reasons, making these products unapproved new drugs.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Marketed without an Approved NDA/ANDA: Products found to contain undeclared sibutramine. Sibutramine was removed from the U.S. market for safety reasons, making these products unapproved new drugs.

Code information

All Lots

Distribution pattern

Nationwide