Class IITerminated in FDA datasetOct 10, 2013

Klaire Labs Interfase Plus; Enzyme Supplement; 120 Vegetarian capsules bottles.

Recalling firm: ProThera, Inc.

Why it was recalled

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

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Compare the exact product and package details with the label you have.

ProductKlaire 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.
UPC709616012284

FDA code information

Lot #'s 0913039, 0913040, and 0413085

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Full FDA record and distribution details

Original product description

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.

Extracted codes and context

TypeCode / valueContext
UPC709616012284bs 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 Cle

Recall details

Recall number
F-0162-2014
Event ID
66553
FDA status
Terminated
Initiated
Oct 10, 2013
Reported
Nov 20, 2013
Classified
Nov 12, 2013
Terminated
Feb 24, 2014
Quantity
Not provided
Location
Reno, NV, United States
Initiation type
Voluntary: Firm initiated
Notification
Letter

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.

FDA source record · F-0162-2014

Data updated September 16, 2026. View official FDA data ↗

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