Nutri-Dyn Calcium D-Glucarate Plus Recalled Due to Mislabeling
Nutri-Dyn Midwest, Inc. is recalling 856 bottles of Calcium D-Glucarate Plus because they were mistakenly labeled as St. John's Wort during production.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II and involves a minor labeling error (mislabeling) without reported illnesses or injuries, fitting the criteria for a moderate severity score.
Plain-English summary
Nutri-Dyn Midwest, Inc. is voluntarily recalling 856 bottles of Nutri-Dyn Calcium D-Glucarate Plus, a dietary supplement containing 60 capsules. The recall is due to a labeling error that occurred during the production of St. John's Wort, Lot 160876, where a number of bottles were mistakenly labeled as Calcium D-Glucarate Plus.
The affected product is identified by Lot 160876 and a manufacturing date of 10/16. The product was distributed in the United States to the following states: AZ, CA, CO, FL, IA, ID, MA, MD, MI, MN, MO, MT, NC, ND, NE, NJ, NV, NY, OH, PA, SC, TX, WI, and WY. It was also distributed in Israel.
Consumers who have purchased this product should stop using it and return it to the place of purchase for a refund. The FDA classifies this recall as Class II, indicating a situation in which there is a reasonable probability that the use of or exposure to the violative product may cause temporary or medically reversible adverse health consequences.
The recalled product
- Product
- Nutri-Dyn Calcium D-Glucarate Plus, Dietary Supplement, 60 Capsules, UPC 7 13757-09611 9
- Manufacturer
- Nutri-Dyn Midwest, Inc.
- Category
- Food — Dietary Supplement
- Hazard
- Affected units
- 856
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- Lot 160876 MFG 10/16
Distribution
Related recalls
Same manufacturer · Nutri-Dyn Midwest, Inc.
See all →- ModerateNutri-Dyn Recalls 5-HTP Extra Strength Capsules Due to Mislabeling
FDA (Food) · 2015-04-15
Same hazard · mis labeling
See all →- ModerateMedline Trach Tube Kit Recalled for Component Labeling Discrepancy
FDA (Devices) · 2026-09-02
- ModerateAVID Medical Recalls Halyard Total Joint Kits for Latex Labeling Deficiency
FDA (Devices) · 2026-09-02
- ModerateOlympus Recalls PowerSeal Sealer Due to Incorrect Outer Box Labeling
FDA (Devices) · 2026-09-02
- HighSura Tanmen Ramen Noodles Recalled for Undeclared Fish Allergens
FDA (Food) · 2026-09-02
- SevereWhite Vein Advanced Alkaloids Chewable Tablets Recall for Excess Active Ingredient
FDA (Food) · 2026-09-02