FDA recall record
Propolis Powder -100% Standardized Bee-Propolis Lot #: 021113-55/60, EXP: 10/14 11# Bag & Lot#: 10081155/60-120612-100, EXP: 12/15, 1# BAG.
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of April 9, 2013. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Propolis Powder -100% Standardized Bee-Propolis Lot #: 021113-55/60, EXP: 10/14 11# Bag & Lot#: 10081155/60-120612-100, EXP: 12/15, 1# BAG.
Reason
Beehive Botanical, Inc is recalling several lots of Propolis 55-60% due to positive identification of Fluvalinate.
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
Propolis Powder -100% Standardized Bee-Propolis Lot #: 021113-55/60, EXP: 10/14 11# Bag & Lot#: 10081155/60-120612-100, EXP: 12/15, 1# BAG.
Code information listed by FDA
10081155/60-120612-100; 021113-55/60
Distribution and firm information
Recalling firm listed by FDA: Beehive Botanicals, Inc.
Firm location listed by FDA: Hayward, WI, United States
Distribution reported by FDA: CA, NY, CANADA
Product quantity listed by FDA: 4,615 LBS
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.