CLASS II Food recall · Reported 12 Jul 2017 · FDA Enforcement Report

Nutri-Dyn Calcium D-Glucarate Plus, Dietary Supplement recalled

Nutri-Dyn Midwest is recalling Nutri-Dyn Calcium D-Glucarate Plus, Dietary Supplement, distributed in 24 states. The recall was initiated on 12 May 2017 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot 160876 MFG 10/16

Quantity recalled856 bottles

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number: F-2423-2017
FDA event ID: 77432
Recalling firm: Nutri-Dyn Midwest, Maple Plain, MN
Brand: Nutri-Dyn Calcium
Classification: Class II
Status: Terminated
Recall initiated: 12 May 2017
FDA classified: 3 Jul 2017
Reported: 12 Jul 2017
Type: Voluntary: Firm initiated
Customers notified by: E-Mail
Reason category: Other Reasons
Product category: Dietary Supplements

Timeline

12 May 2017	Recall initiated by company
3 Jul 2017	Classified by FDA	+52 days
12 Jul 2017	Published in enforcement report	+9 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

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

Product as listed by the FDA

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

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

Arizona California Colorado Florida Iowa Idaho Massachusetts Maryland Michigan Minnesota Missouri Montana North Carolina North Dakota Nebraska New Jersey Nevada New York Ohio Pennsylvania

Questions about this recall

Is Nutri-Dyn Calcium D-Glucarate Plus, Dietary Supplement recalled?

Yes. Nutri-Dyn Midwest recalled Nutri-Dyn Calcium D-Glucarate Plus, Dietary Supplement on 12 May 2017. The recall is Class II and its status is Terminated. Recall number F-2423-2017.

Why was it recalled?

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

Which lots are affected?

Lot 160876 MFG 10/16

Where was it sold?

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

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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