FDA recalls · F-0161-2014
ProThera, Inc. recall
- FoodKlaire 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
- ReasonProThera was notified by enzymes provided by Specialty Enzymes within the last 3-6 months may be contaminated with chloramphenicol.
- ClassClass II: the food could cause temporary or treatable health problems
- StatusClosed by FDA, ended 2014-02-24
- DatesFirm started it 2013-10-10. In FDA's enforcement report 2013-11-20.
- Sold inUS 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.
- Amount243,851
- CodesLot #' 313127
- FirmProThera, Inc., Reno, NV · Voluntary: Firm initiated
Products we list
None. We tie a recall to a product only by a barcode printed in the recall, and this one names none we list. That does not mean the recalled food is missing from our listings.
From FDA's enforcement report, via openFDA (CC0): raw data for this recall. FDA's own Enforcement Report search finds it by its number, F-0161-2014. Class meanings: FDA.