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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 94782

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

Open FDA event record

Event summary

Timeline bucket
June 05, 2024
Product types
Drug
Classifications
Class I and Class II
Statuses
Terminated
Recalling firm wording
Homeocare Laboratories, 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

STELLALIFE VEGA Oral Care, Spray, Unflavored, 1 fl oz (30 ml) bottles, Distributed by: StellaLife, 22875 NE 191 Street, Suite 500, Aventura, FL 33180, NDC 69685-121-01

D-0609-2024
Recall number
D-0609-2024
Initiated
June 05, 2024
Classification
Class I
Status
Terminated
Quantity
31,811 x 1 fl. oz. spray bottle

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0
Microbial Contamination

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Microbial Contamination of Non-Sterile Products: multiple Bacillus species organisms

Code information

Lot # 2552, exp. date 02-28-2026

Distribution pattern

Nationwide to 60 Physician offices

drug · product 2 of 2

STELLALIFE ADVANCED FORMULA Peppermint, VEGA Oral Care, Rinse, 16 fl oz (473 ml), Distributed by: StellaLife, 2875 NE 191 Street, Suite 500, Aventura, FL 33180, NDC 69685-143-16

D-0610-2024
Recall number
D-0610-2024
Initiated
June 05, 2024
Classification
Class II
Status
Terminated
Quantity
31,110 x 16 fl. oz. bottle

App-derived interpretation

Microbial contamination reason.microbial_contamination · v1.0.0
Microbial Contamination

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Microbial Contamination of Non-Sterile Products: presence of Terribacillus species organism

Code information

Lot # 2550, exp. date 02-28-2026

Distribution pattern

Nationwide to 60 Physician offices