FDA recall record
GL Completia, 90 vcaps HDPE Bottle in a Box 12
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 February 26, 2015. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
GL Completia, 90 vcaps HDPE Bottle in a Box 12
Reason
Nature's Way (NW) is voluntary recalling a number of products because the raw material supplier informed them that enzymes in the blend they provided to NW may contain the antibiotic 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.
GL Completia, 90 vcaps HDPE Bottle in a Box 12
Code information listed by FDA
20009982
Distribution and firm information
Recalling firm listed by FDA: Schwabe North America, Inc.
Firm location listed by FDA: Green Bay, WI, United States
Distribution reported by FDA: US: AK, AL, AR, AZ, CA, CI, CT, DC, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, NS, NT, NC, ND, NE, NH, NJ, NM, NV, NY, H, OK, OR, PA, PR, RI,SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY. OUS: South Korea, Ghana, Romania and Singapore.
Product quantity listed by FDA: 4666
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.