FDA recall record

New Sun Dietary Supplement, 100 capsule bottle, New Sun, Inc recall — FDA F-1880-2013

Positive E.coli

Class IIclassification
F-1880-2013official record ID
Sep 18, 2013report date

Recall record at a glance

Official recordF-1880-2013
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmNew Sun Inc.
Report dateSep 18, 2013
Recall initiation dateJul 22, 2013
Quantity38,900 capsules
LocationHendersonville, NC, United States

Official product description

New Sun JLB Combination, Dietary Supplement, 100 capsule bottle, New Sun, Inc., Hendersonville, NC 1-800-544-0777 www.newsun.net Product No. 78-1

Why the product was recalled

Positive E.coli

Distribution information

AL, CA, CO, FL GA, HI, ID, IL, IN, IA, KY, ME, MD, MA, MI, MN, MO, NH, NJ, NM, NY, NC, OH, PA, RI, SC, SD, TN, TX, VA, WA

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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