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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 71912

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

Open FDA event record

Event summary

Timeline bucket
August 06, 2015
Product types
Drug
Classifications
Class I
Statuses
Terminated
Recalling firm wording
Blue Square Market, 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

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

LiDa DAIDAIHUA (also packaged as LiDa DAIDAIHUAJIAONANG), capsules, packaged in 1.6oz box 30 capsules per box, Kunming Dali Industry & Trade Co., Ltd

D-0296-2016
Recall number
D-0296-2016
Initiated
August 06, 2015
Classification
Class I
Status
Terminated
Recalling firm
Blue Square Market, Inc.
Quantity
25 boxes

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Marketed Without An Approved NDA/ANDA: presence of undeclared Sibutramine and Phenolphthalein.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Marketed Without An Approved NDA/ANDA: presence of undeclared Sibutramine and Phenolphthalein.

Code information

all lots

Distribution pattern

Nationwide

drug · product 2 of 2

KABOOM action strips, Sexual Performance Strips, packaged in 6.4oz box 12 strips per box, Nutrology USA LLC

D-0297-2016
Recall number
D-0297-2016
Initiated
August 06, 2015
Classification
Class I
Status
Terminated
Recalling firm
Blue Square Market, Inc.
Quantity
132 boxes

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Marketed Without An Approved NDA/ANDA: presence of undeclared Sulfoaildenafil.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Marketed Without An Approved NDA/ANDA: presence of undeclared Sulfoaildenafil.

Code information

all lots

Distribution pattern

Nationwide