Food Recall Check
Class II · Moderate risk Terminated Initiated May 12, 2017 (9 years ago)

Nutri-Dyn Calcium D-Glucarate Plus recall

Recalled by Nutri-Dyn Midwest, Inc. · Maple Plain, MN, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

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

A label that does not match the product can hide an ingredient someone must avoid, or show a wrong use-by date. All labeling errors recalls.

What was recalled

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

Quantity: 856 bottles

Food: Dietary supplements

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

Lot 160876 MFG 10/16

Where it was sold

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

FDA's distribution note: 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

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Nutri-Dyn Midwest, Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
May 12, 2017
In FDA report of
Jul 12, 2017
Terminated
Sep 20, 2017
FDA recall number
F-2423-2017 · event 77432
Official record
FDA enforcement report search

Other recalls by Nutri-Dyn Midwest, Inc.

Class III · Low risk Terminated Labeling

Nutri-Dyn

Reason Nutri-Dyn has initiated a recall due to mislabeling. During production of CoQ-10, Lot #140186, one or more bottles were mistakenly labeled as 5-HTP Extra Strength.

Nutri-Dyn Midwest, Inc. 13 states F-1922-2015

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