F-0161-2014 Class II Terminated
FDA food recall F-0161-2014 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: 243,851.
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
- 243,851
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
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 #' 313127