Food Recall Check
Class II · Moderate risk Terminated Initiated Nov 6, 2013 (13 years ago)

Pro Thera Dual Detox Dietary Supplement recall

Recalled by ProThera, Inc. · Reno, NV, United States

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

Why it was recalled

Firm was notified by supplier of the enzyme Xylanase that it was contaminated with chloramphenicol.

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

What was recalled

Pro Thera Dual Detox Dietary Supplement; 60 capsules; Chlorella - 500 mg; Broccoli Sprout, dried extract - 60 mg; Enzyme Blend - supplying Beta-Glucanase, Cellulase, Protease, Hemicellulase, Phytase and Xylanase Manufactured by ProThera, Reno, NV,

Quantity: 54, 503 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.

Lot B3222, product code DTX

Where it was sold

FDA's distribution note: US and Canada, Germany, Great Britain, Hong Kong, Malaysia, Mexico, Philippines, Russia, Singapore, South Korea , Spain

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
ProThera, Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Nov 6, 2013
In FDA report of
Nov 27, 2013
Terminated
Jul 16, 2014
FDA recall number
F-0180-2014 · event 66793
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.

Class II · Moderate risk Terminated Other

Lifeforce Medical Institute Ultra Power

Reason Firm was notified by supplier of the enzyme Xylanase that it was contaminated with chloramphenicol.

ProThera, Inc. F-0179-2014

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