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FDA recall record

Nutri-Dyn Calcium D-Glucarate Plus, Dietary Supplement, 60 Capsules, UPC 7 13757-09611 9

Recall F-2423-2017Class IITerminatedMay 12, 2017

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 September 20, 2017. openFDA does not treat this as a live recall-status tracker.

Product described in an FDA recall

Nutri-Dyn Calcium D-Glucarate Plus, Dietary Supplement, 60 Capsules, UPC 7 13757-09611 9

Reason

During production of St. John's Wort, Lot 160876, a number of bottles were mistakenly labeled as Calcium D-Glucarate Plus

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.

  • Nutri-Dyn Calcium D-Glucarate Plus, Dietary Supplement, 60 Capsules, UPC 7 13757-09611 9

Code information listed by FDA

Lot 160876 MFG 10/16

Distribution and firm information

Recalling firm listed by FDA: Nutri-Dyn Midwest, Inc.

Firm location listed by FDA: Maple Plain, MN, United States

Distribution reported by FDA: US: AZ, CA, CO,, FL, IA, ID, MA, MD, MI, MN, MO, MT, NC, ND, NE, NJ, NV, NY, OH, PA SC, SC, TX, WI, WY. OUS: ISRAEL

Product quantity listed by FDA: 856 bottles

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.