FDA recall record
Herbal Tea Variety 120 ml/pouch, 40 pouches/case
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 June 14, 2017. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Herbal Tea Variety 120 ml/pouch, 40 pouches/case
Reason
US Deer Antler Export and Import is recalling a variety of Herbal Teas because they may be contaminated with Clostridium botulinum
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.
Herbal Tea Variety 120 ml/pouch, 40 pouches/case
Code information listed by FDA
Herbal Tea Variety Batches prepared on premise between 3/1/17 and 4/30/17
Distribution and firm information
Recalling firm listed by FDA: U S Deer Antlers Export & Import
Firm location listed by FDA: Los Angeles, CA, United States
Distribution reported by FDA: US: CA, TX, NC, NY, VA, HI, GA, WA, IL, PA, OK, MO, MD, NJ. Korea.
Product quantity listed by FDA: 9,480 units
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.