Exact FDA event identifier

Event 83631

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

Open FDA event record

Event summary

Timeline bucket: August 28, 2019
Product types: Food
Classifications: Class III
Statuses: Terminated
Recalling firm wording: Jivan Shakti 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

Device root-cause evidence is not applicable to this event. No grouped product has the official product type device; this is not an unavailable-enrichment finding.

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

Plastic Bottles labeled with: "Ancient Youth Secret - Since 500 B.C., DR. NARAM'S RASAYANA D TABLET, Calcium Supplement with Vitamin D*, Dietary Supplement, 60 Tablets, FOR EXPORT ONLY, Imported & Distributed by: Jivan Shakti INC, 933 South Street, Peekskill, NY 10566, Manufactured by: Reve Pharma, Plot No-78, STICE, Sinnar, Nashik-422 112, Maharashtra, India, Mfr. Lic. No.: NK/AYU/004/08, Batch No: RST-010, Mfr. Date: 05/2018, Exp. Date: 04/2021, Dose: 1 Tab AM, 1 Tab PM"

F-2144-2019

Recall number: F-2144-2019
Initiated: August 28, 2019
Classification: Class III
Status: Terminated
Recalling firm: Jivan Shakti Inc.
Quantity: 790 bottles

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0

Product label declares Vitamin D3 at 200 IU per serving. FDA sample analysis revealed no Vitamin D in product.

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Product label declares Vitamin D3 at 200 IU per serving. FDA sample analysis revealed no Vitamin D in product.

Code information

Batch No: RST-010, Mfr. Date: 05/2018, Exp. Date: 04/2021

Distribution pattern

Product was distributed in: AZ, CA, CT, FL, GA, IL, IN, MA, MD, MI, MN, NC, NJ, NY, OH, PA, TN, TX, VA, WA