FDA recall record
Xylanase 150,000XU, powder, enzyme, 100 gm. Product 13A
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 16, 2014. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Xylanase 150,000XU, powder, enzyme, 100 gm. Product 13A
Reason
The products may be contaminated with Chloramphenicol.
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.
Xylanase 150,000XU, powder, enzyme, 100 gm. Product 13A
Code information listed by FDA
Lot ALI13157-11; re-evaluation date 12/6/2014 **sample only - not tested
Distribution and firm information
Recalling firm listed by FDA: American Laboratories Inc
Firm location listed by FDA: Omaha, NE, United States
Distribution reported by FDA: Distribution was made to IA, UT, NV, NE and CA.
Product quantity listed by FDA: 1 sample bottle, 100 gm
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.