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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 87919

1 recalled-product record grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
May 12, 2021
Product types
Food
Classifications
Class II
Statuses
Ongoing
Recalling firm wording
Hi Tech Pharmaceuticals

Dossier provenance

Source snapshots represented here

  • openFDA Food 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

1 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.

food · product 1 of 1

Lipodrene With 25mg Ephedra Extract 100CT UPC 8 57084 00056 9

F-0647-2021
Recall number
F-0647-2021
Initiated
May 12, 2021
Classification
Class II
Status
Ongoing
Recalling firm
Hi Tech Pharmaceuticals
Quantity
19,068/100 ct bottles

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
The firm was notified by the FDA that the product contains the unapproved food additive 1,4-dimethylamylamine (DMAA).

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

The firm was notified by the FDA that the product contains the unapproved food additive 1,4-dimethylamylamine (DMAA).

Code information

Lot # 001211197, Exp. 12/25

Distribution pattern

The product was shipped to the following states: AL, AZ, CA, CO, CT, FL, GA, IA, ID, IL, IN, KS, LA, MA, MD, ME, MI, MO, MS, MT, NC, NE, NE, NJ, NM, NV, NY, OH, OK, OR, PA, PR, TN, TX, UT, VA, VT, WA & WI.