Class IITerminated in FDA datasetOct 10, 2013

Klaire Labs Interfase; Enzyme Supplement; Packaged in 60 and 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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ProductKlaire Labs Interfase; Enzyme Supplement; Packaged in 60 and 120 Vegetarian capsules bottles. UPC 60 ct.- 7 0961 012270 7; UPc 120 ct. - 7 09616-01229 1 Manufactured by ProThera, Inc., , Klaire Labs is a division of ProThera Reno, NV 89521

FDA code information

Lot #' 313127

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Full FDA record and distribution details

Original product description

Klaire Labs Interfase; Enzyme Supplement; Packaged in 60 and 120 Vegetarian capsules bottles. UPC 60 ct.- 7 0961 012270 7; UPc 120 ct. - 7 09616-01229 1 Manufactured by ProThera, Inc., , Klaire Labs is a division of ProThera Reno, NV 89521

Recall details

Recall number
F-0161-2014
Event ID
66553
FDA status
Terminated
Initiated
Oct 10, 2013
Reported
Nov 20, 2013
Classified
Nov 12, 2013
Terminated
Feb 24, 2014
Quantity
243,851
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-0161-2014

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

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