FDA recall record
Pectinase 3,500 ENDO-PG/G, powder, enzyme, 100 gm. Product 70A
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
Pectinase 3,500 ENDO-PG/G, powder, enzyme, 100 gm. Product 70A
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.
Pectinase 3,500 ENDO-PG/G, powder, enzyme, 100 gm. Product 70A
Code information listed by FDA
Lot ALI13157-09; re-evaluation date 12/6/2014. **sample only - not tested On 10/22/2013 American Laboratories provided CFSAN a customer distribution list for the Chloramphenicol Contamination. This spreadsheet listed the base concentrate levels. The data was highlighted: Green, Yellow, Red and Orange.The spreadsheet
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: one 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.