The Recall Desk
HighFDA (Food)·F-0161-2014·Announced 2013-11-20

Klaire Labs Interfase Enzyme Supplement Recalled for Chloramphenicol Contamination

ProThera, Inc. is recalling Klaire Labs Interfase enzyme supplements because the enzymes used may be contaminated with chloramphenicol.

What this means for you

Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.

Our severity reasoning: The recall involves a potential contamination with chloramphenicol, a high-risk pathogen/chemical, without reported illness, fitting the High severity criteria.

Plain-English summary

ProThera, Inc. is recalling Klaire Labs Interfase enzyme supplements, packaged in 60 and 120 vegetarian capsule bottles. The recall involves Lot #313127, with a total of 243,851 units affected.

The recall was initiated after ProThera was notified that the enzymes provided by Specialty Enzymes within the last 3-6 months may be contaminated with chloramphenicol. The product was distributed in the US and Australia, Azerbaijan, Brazil, Canada, Germany, Great Britain, Hong Kong, Ireland, Japan, Malaysia, Malta, Mexico, New Zealand, Panama, Philippines, Russia, South Korea, Spain, Switzerland, and Thailand.

Consumers should stop using the recalled product and return it to the place of purchase for a refund or follow instructions provided by the manufacturer.

The recalled product

Product
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
Manufacturer
ProThera, Inc.
Affected units
243,851

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (1)

  • Lot #' 313127

Distribution

Distribution scope not specified by the agency.

Part of a larger recall action

This product is one of 5 recalled by ProThera, Inc. under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 5 products in this recall →