Plastic Bottles labeled with recall
Recalled by Jivan Shakti Inc. · Peekskill, NY, United States
Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.
Why it was recalled
Product label declares Vitamin D3 at 200 IU per serving. FDA sample analysis revealed no Vitamin D in product.
A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.
What was recalled
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"
Quantity: 790 bottles
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
Batch No: RST-010, Mfr. Date: 05/2018, Exp. Date: 04/2021
Where it was sold
Arizona California Connecticut Florida Georgia Illinois Indiana Massachusetts Maryland Michigan Minnesota North Carolina New Jersey New York Ohio Pennsylvania Tennessee Texas Virginia Washington
FDA's distribution note: Product was distributed in: AZ, CA, CT, FL, GA, IL, IN, MA, MD, MI, MN, NC, NJ, NY, OH, PA, TN, TX, VA, WA
Low risk, but check. Class III means the product is unlikely to make anyone ill but breaks an FDA rule, often a labeling one. If your package matches, the store will normally refund it. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- Jivan Shakti Inc.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Aug 28, 2019
- In FDA report of
- Sep 18, 2019
- Terminated
- Jan 14, 2021
- FDA recall number
- F-2144-2019 · event 83631
- Official record
- FDA enforcement report search