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ProThera, Inc.
FDA recall F-0158-2014 · Class II · reported 2013-11-20 · Terminated
- Product
- 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
- ProThera was notified by enzymes provided by Specialty Enzymes within the last 3-6 months may be contaminated with chloramphenicol.
- Quantity
- 27,480
- Distribution
- 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.
- Firm location
- NV, United States
- Initiated
- Voluntary: Firm initiated
- First notice
- Letter
- Recall started
- 2013-10-10
- Terminated
- 2014-02-24
- Code info
- Lot F3994
Source: U.S. Food and Drug Administration, openFDA Food Enforcement database (openFDA Food Enforcement, imported 2026-09). The FDA does not validate openFDA data for completeness or accuracy. This is a record of an enforcement action, not safety advice.