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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 87653

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

Open FDA event record

Event summary

Timeline bucket
March 30, 2021
Product types
Drug
Classifications
Class II
Statuses
Ongoing
Recalling firm wording
Na Na Collection

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

PremierZen Platinum 5000, Packaged in paper packaging with a pill blister, 1 capsule per box, Distributed by New Premier Group Los Angeles CA 90006

D-0353-2021
Recall number
D-0353-2021
Initiated
March 30, 2021
Classification
Class II
Status
Ongoing
Recalling firm
Na Na Collection
Quantity
N/A

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Marketed without Approved NDA/ANDA: FDA analysis results obtained the presence of tadalafil and/or sildenafil.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Marketed without Approved NDA/ANDA: FDA analysis results obtained the presence of tadalafil and/or sildenafil.

Code information

Lot #: GATCO 01671, Exp Date 12/30/2024 Serial # 728175421856

Distribution pattern

Nationwide with the United States

drug · product 2 of 2

Triple SupremeZen Gold 3500, Packaged in paper packaging with a pill blister,1 capsule per box, Distributed by VIEW LIFE Distributors Los Angeles CA 90005 UPC 7 15122 05089 4

D-0354-2021
Recall number
D-0354-2021
Initiated
March 30, 2021
Classification
Class II
Status
Ongoing
Recalling firm
Na Na Collection
Quantity
N/A

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Marketed without Approved NDA/ANDA: FDA analysis results obtained the presence of tadalafil and/or sildenafil.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Marketed without Approved NDA/ANDA: FDA analysis results obtained the presence of tadalafil and/or sildenafil.

Code information

Lot #: GATCO 1805, Exp. Date 12/30/2024 Serial # 715122050894

Distribution pattern

Nationwide with the United States