The Recall Desk
HighFDA (Food)·F-0162-2014·Announced 2013-11-20

Klaire Labs Interfase Plus Enzyme Supplement Recalled for Chloramphenicol Contamination

ProThera, Inc. is recalling Klaire Labs Interfase Plus enzyme supplements because the enzymes 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 substance, but the source text does not report any illnesses or injuries, fitting the 'High' severity criteria for risk-of-harm products where injury has not yet been reported.

Plain-English summary

ProThera, Inc. is recalling Klaire Labs Interfase Plus enzyme supplements. The product is sold in 120 vegetarian capsule bottles with UPC 7 09616 01228 4. The recall affects specific lot numbers: 0913039, 0913040, and 0413085.

The recall was initiated because ProThera was notified that 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 contact ProThera, Inc. for further instructions. The source text does not specify the exact action consumers should take beyond the standard recall notification.

The recalled product

Product
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 produc
Manufacturer
ProThera, Inc.

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 (3)

  • Lot #'s 0913039
  • 0913040
  • and 0413085

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 →