XymoZyme dietary supplement recall

Recalled by Health Wright Products Inc · Clackamas, OR, United States

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

Why it was recalled

Dietary supplement products are recalled because they were made from ingredient that was contaminated with Chloramphenicol.

See the recall's own reason text for the specifics. All other reasons recalls.

What was recalled

XymoZyme, dietary supplement, packaged 60 capsules per bottte, 120 capsules per bottle, sold under brand ZYMOGEN.

Quantity: 7890 bottles

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.

60 count bottle: LOT# 1207301D, EXP 03/14 (means March 2014); LOT# 1221501D, EXP 08/14 (means August 2014); LOT# 1229205D, EXP 10/14 (means October 2014); 120 count bottle: LOT# 1207301H; EXP 03/14 (means March 2014); LOT# 1221501H, EXP 08/14 (means August 2014); LOT# 1229205H, EXP 10/14 (means October 2014);

Where it was sold

California Florida Oregon Utah

FDA's distribution note: Distributed to California, Florida, Oregon, Utah, and Mexico

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: Health Wright Products Inc
Initiated by: Voluntary: Firm initiated
Recall initiated: Oct 25, 2013
In FDA report of: Feb 5, 2014
Terminated: Mar 2, 2015
FDA recall number: F-1460-2014 · event 66843
Official record: FDA enforcement report search

Also recalled with it (8 more products)

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

Class II · Moderate risk Terminated Other Oct 25, 2013