Food Recall Check
Class II · Moderate risk Terminated Initiated Mar 13, 2015 (12 years ago)

Klaire Labs Ther-Biotic FACTOR 6 100+ Billion CFU's Multi-Species… 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 is recalling three lots of Ther-Biotic dietary supplements due to reports of shards of blue glass found in the bottles, not the in supplement.

Hard or sharp fragments can cut the mouth or throat, break teeth or cause choking. They usually come from equipment wear or packaging on the production line. All foreign material recalls.

What was recalled

Klaire Labs Ther-Biotic FACTOR 6 100+ Billion CFU's Multi-Species Probiotic Supplement 60 Vegetarian Capsules. UPC 7 09616 01248 2 Manufactured by ProThera Inc . Klaire Labs is a division of ProThera, Reno, NV.

Quantity: lot H4496 = 1,337 total bottles; lot K4780 = 1,336 total 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.

K-TF6 (60 capsules) Lot Number: H4496, Exp 10/15 and K4786, Exp 1/16.

Where it was sold

Nationwide.

FDA's distribution note: Nationwide and to Azerbaijan, Canada, China, Germany, Great Britain,Hong Kong, Indonesia, Japan, Malaysia, Mexico, Panama, Russia, Singapore, Spain, Switzerland, Ukraine.

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
Mar 13, 2015
In FDA report of
Apr 22, 2015
Terminated
Jul 1, 2015
FDA recall number
F-1953-2015 · event 70761
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.

Other recalls by ProThera, Inc.

Class II · Moderate risk Terminated Other

Pro Thera Dual Detox Dietary Supplement

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

ProThera, Inc. F-0180-2014
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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