Food Recall Check
Class II · Moderate risk Terminated Initiated Jul 22, 2013 (13 years ago)

New Sun Immune 101 recall

Recalled by New Sun Inc · Hendersonville, NC, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Positive E.coli

Pathogen: E. coli

Shiga toxin-producing E. coli (such as O157:H7) can cause severe illness and kidney failure.

The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.

What was recalled

New Sun Immune 101, Dietary Supplement 360 Capsule bottles and 100 capsule bottles, New Sun, Inc, Hendersonville NC 28792 1-800-544-0777 www.newsun.net product No. 74-0

Quantity: 61,840 capsules

Food: Dietary supplements

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.

07237 and 07238

Where it was sold

Alabama California Colorado Florida Georgia Hawaii Iowa Idaho Illinois Indiana Kentucky Massachusetts Maryland Maine Michigan Minnesota Missouri North Carolina New Hampshire New Jersey New Mexico New York Ohio Pennsylvania Rhode Island South Carolina South Dakota Tennessee Texas Virginia Washington

FDA's distribution note: 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

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. 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
New Sun Inc
Initiated by
Voluntary: Firm initiated
Recall initiated
Jul 22, 2013
In FDA report of
Sep 18, 2013
Terminated
Nov 21, 2013
FDA recall number
F-1881-2013 · event 65783
Official record
FDA enforcement report search

Also recalled with it (1 more product)

FDA files each product of one recall action separately; these share the same FDA event.

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