CLASS II Food recall · Reported 20 Nov 2013 · FDA Enforcement Report

Klaire Labs Interfase Plus recalled by ProThera

ProThera is recalling Klaire Labs Interfase Plus. The recall was initiated on 10 Oct 2013 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot #'s 0913039, 0913040, and 0413085

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number: F-0162-2014
FDA event ID: 66553
Recalling firm: ProThera, Reno, NV
Brand: Klaire Labs
Classification: Class II
Status: Terminated
Recall initiated: 10 Oct 2013
FDA classified: 12 Nov 2013
Reported: 20 Nov 2013
Type: Voluntary: Firm initiated
Customers notified by: Letter
Reason category: Other Reasons
Product category: Dietary Supplements

Timeline

10 Oct 2013	Recall initiated by company
12 Nov 2013	Classified by FDA	+33 days
20 Nov 2013	Published in enforcement report	+8 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

ProThera was notified by enzymes provided by Specialty Enzymes within the last 3-6 months may be contaminated with chloramphenicol.

Product as listed by the FDA

Klaire Labs Interfase Plus; Enzyme Supplement; 120 Vegetarian capsules bottles. UPC 7 09616 01228 4 Manufactured by ProThera, Inc., , Klaire Labs is a division of ProThera Reno, NV 89521 Notation: Product #6 Clean Cut Enzyme wasn't entered into RES because the product never left the warehouse.

Where it was distributed

US and Australia, Azerbaijan, Brazil, Canada, Germany, Great Britain, Hong Kong, Ireland (Eire, Japan, Malaysia, Malta, Mexico, New Zealand, Panama, Philippines, Russia, South Korea, Spain, Switzerland, Thailand.

Questions about this recall

Why was it recalled?

ProThera was notified by enzymes provided by Specialty Enzymes within the last 3-6 months may be contaminated with chloramphenicol.

Which lots are affected?

Lot #'s 0913039, 0913040, and 0413085

Where was it sold?

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

4 other products · FDA event 66553

This product is part of a recall event; the main page for the event is Klaire Labs Interfase recalled by ProThera.

Reported	Class	Recall	Company	Reason	Where
20 Nov 2013	CLASS II	Klaire Labs Interfase recalled by ProTheraKlaire Labs	ProThera	Packaging Defects	NV
20 Nov 2013	CLASS II	Klaire Labs Vital-Zymes Chewable recalled by ProTheraKlaire Labs	ProThera	Other	NV
20 Nov 2013	CLASS II	Serralase Enzyme Supplements recalled by ProTheraSerralase Enzyme	ProThera	Packaging Defects	NV
20 Nov 2013	CLASS II	Klaire Labs Vital-Zymes complete recalled by ProTheraKlaire Labs	ProThera	Other	NV

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All 11

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