F-0158-2014 Class II Terminated

Recalled by ProThera, Inc. — Reno, NV

FDA food recall F-0158-2014 was initiated by ProThera, Inc. on October 10, 2013 and is designated Class II. Reason for recall: ProThera was notified by enzymes provided by Specialty Enzymes within the last 3-6 months may be contaminated with chloramphenicol. The recall status is terminated (terminated February 24, 2014). Affected quantity: 27,480.

Recall Details

Product Type
Food
Report Date
November 20, 2013
Initiation Date
October 10, 2013
Termination Date
February 24, 2014
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
27,480

Product Description

Serralase Enzyme Supplements; Packaged in 90 and 180 tablet bottled UPC - 90 count: 8 28054 00542 6 UPC- 180 count 8 28054 00149 7; Manufactured by: ProThera, Inc., Reno, NV 89521

Reason for Recall

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

Distribution Pattern

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.

Code Information

Lot F3994