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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 81788

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

Open FDA event record

Event summary

Timeline bucket
December 13, 2018
Product types
Food
Classifications
Class II
Statuses
Terminated
Recalling firm wording
ProThera, Inc. dba SFI USA

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

Klaire Labs Reduced L-Glutathione 150 mg capsules, single capsule dose 100 vegetarian capsules SKU V799-10 UPC Code: 7 09616 79910 9

F-1186-2019
Recall number
F-1186-2019
Initiated
December 13, 2018
Classification
Class II
Status
Terminated
Quantity
139 bottles

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Mis-packaging; product is labeled as Reduce L-Glutathione but actually contains Lithium Orotate.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Mis-packaging; product is labeled as Reduce L-Glutathione but actually contains Lithium Orotate.

Code information

FG Lot: 2018210303 Expiration: 05/2020

Distribution pattern

US distribution to the following: AL, AZ, CA, KS, LA, MI, MO, NH, NJ, NY, OR, PA, TX, and WA Foreign distribution to the following: Netherlands, Great Britain, and Korea