Class IITerminated in FDA datasetRecall initiated May 12, 2017

Nutri-Dyn Calcium D-Glucarate Plus, Dietary Supplement, 60 Capsules

Recalling firm: Nutri-Dyn Midwest, Inc.

Why it was recalled

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

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Sep 20, 2017.

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ProductNutri-Dyn Calcium D-Glucarate Plus, Dietary Supplement, 60 Capsules, UPC 7 13757-09611 9
UPC713757096119

FDA code information

Lot 160876 MFG 10/16

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Full FDA record and distribution details

Original product description

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

Extracted codes and context

TypeCode / valueContext
UPC713757096119Nutri-Dyn Calcium D-Glucarate Plus, Dietary Supplement, 60 Capsules, UPC 7 13757-09611 9

Original FDA recall reason

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

Recall details

Recall number
F-2423-2017
Event ID
77432
FDA status
Terminated
Initiated
May 12, 2017
Reported
Jul 12, 2017
Classified
Jul 3, 2017
Terminated
Sep 20, 2017
Quantity
856 bottles
Location
Maple Plain, MN, United States
Initiation type
Voluntary: Firm initiated
Notification
E-Mail

Where it was distributed

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

FDA source record · F-2423-2017

Data updated September 16, 2026. View official FDA data ↗

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