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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 62786

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

Open FDA event record

Event summary

Timeline bucket
December 08, 2009
Product types
Food
Classifications
Class II
Statuses
Terminated
Recalling firm wording
GMP Laboratories of America Inc

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

Dietary supplement. Product is labeled as :" Rescue Me***911 Damage Control***brantley living herbal formulas***HERBAL SUPPLEMENT 15 INDIVIDUAL PACKETS 4 VEGAN CAPSULES PER PACKET (2-368mg/2-584mg Each)***DISTRIBUTED EXCLUSIVELY BY: Living Herbal Pharmacy, LLC PO Box 56-2410, Miami, FL 33256-2410***".

F-2297-2012
Recall number
F-2297-2012
Initiated
December 08, 2009
Classification
Class II
Status
Terminated
Quantity
1027 boxes

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0
mispackaged

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

The firm recalled because the product lot contained mispackaged product wherein some capsules were missing from the finished packaged product.

Code information

LOT 2448 BEST BY 10/12

Distribution pattern

US States nationwide.

Field note

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