US Food Recall Atlas

A single recall record, as the agency published it.

Recall mapAll recalls → F-0161-2014

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 ProThera, Inc. · reported 2013-11-20

Terminated This recall has been closed out by the agency.

Reason for recall
ProThera was notified by enzymes provided by Specialty Enzymes within the last 3-6 months may be contaminated with chloramphenicol.
Classification
Class II
Recall initiated
2013-10-10
Reported by the agency
2013-11-20
Closed out (terminated)
2014-02-24
Recalling firm
ProThera, Inc.
Reno, NV
United States

This is the firm that issued the recall — commonly a distributor or processor. It is not the origin of contamination.

Distribution (the agency's own words)
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.
States we parsed from that text
AL AR DC DE FL GA KY LA MD MS NC OK SC TN TX VA WVour expansion

The agency wrote a broader phrase; these state names are ours, not theirs. Parse method region_expansion, confidence medium.

Food category
Dietary supplementsderived

Assigned by a reviewed keyword rulebook over the product description, not by the agency.

Recall type
Voluntary: Firm initiated
Recall number
F-0161-2014

This page reproduces a record published by the US Food and Drug Administration. It is not real-time: recalls typically appear in FDA's Enforcement Report weeks after they begin — a median of 40 days, see publication lag. For current food safety information consult FDA and USDA FSIS directly.