Why it was recalled
ProThera was notified by enzymes provided by Specialty Enzymes within the last 3-6 months may be contaminated with chloramphenicol.
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
Lot numbers, UPCs & expiration codes
Lot F3994
Where it was sold
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.
What to do if you have this product
- Compare the brand, size, and lot/UPC codes on your package with the codes above.
- If it matches, don't eat it. Return it to the store for a refund or throw it away.
- Wash surfaces and containers that touched the product.
- If you feel sick after eating it, contact your doctor. In an emergency call 911.
Recall details
- Recall number
- F-0158-2014
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- Oct 10, 2013
- FDA report date
- Nov 20, 2013
- Quantity
- 27,480
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- ProThera, Inc.
Original FDA data
Every field from FDA enforcement report F-0158-2014, exactly as published.
Show all FDA fields
- City
- Reno
- State
- NV
- Status
- Terminated
- Country
- United States
- Event ID
- 66553
- Address
- 10439 Double R Blvd
- Code information
- Lot F3994
- Postal code
- 89521-8905
- Report date
- Nov 20, 2013
- Product type
- Food
- Recall number
- F-0158-2014
- Classification
- Class II
- Recalling firm
- ProThera, Inc.
- Product quantity
- 27,480
- Termination date
- Feb 24, 2014
- Reason for recall
- ProThera was notified by enzymes provided by Specialty Enzymes within the last 3-6 months may be contaminated with chloramphenicol.
- Voluntary / mandated
- Voluntary: Firm initiated
- 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
- 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.
- Recall initiation date
- Oct 10, 2013
- Initial firm notification
- Letter
- Center classification date
- Nov 12, 2013