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Dietary supplements Recalls

Are there any recent dietary supplements recall records?

24 recent FDA-listed ongoing recall records in this snapshot.FDA data updated September 16, 2026 · Snapshot assessed September 18, 2026
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“Recent ongoing” means initiated within 365 days of September 18, 2026, FDA status “Ongoing,” and no termination date. This snapshot cannot confirm what is active today. 23 older records still list “Ongoing.”

1,310 FDA product recordsLatest initiation: Aug 11, 2026

Same product name.
Different batch.
Check the label.

Dietary supplements recall history

Initiated in 2023. Latest and historical records, ordered by initiation date (newest first). FDA status appears on each record.

80 recall recordsPage 1 of 7
Class III
FDA status: Terminated

Brand Name: SUPREX Plant Based Nutrition. Product Name: Carb & Sugar Block. Product Size: 120 Vegetable Cellulose…

FDA lab analysis of product sampled revealed Chromium content was determined subpotent as 16 mcg/serving or 16% of declared.

OtherView details →
Class II
FDA status: Terminated

Spring Valley Biotin & Collagen Liquid, Natural Berry Flavor, 15000 mcg, Dietary Supplement 29 doses 1 fl oz (29mL)

Potential mold contamination

Mold / spoilageView details →
Class II
FDA status: Terminated

Garden of Life, FYI ULTRA, ULTIMATE Joint & Cartilage Formula, Whole Food Dietary Supplement, 120 Ultra Zorbe…

Undeclared Soy.

Undeclared allergenView details →
Class II
FDA status: Terminated

Garden of Life, RM-10, Organically Grown Mushrooms, 60 Vegetarian Caplets, Whole Food Dietary Supplement

Undeclared Soy.

Undeclared allergenView details →
Class II
FDA status: Terminated

Garden of Life, RM-10 ULTRA, Ultimate Immune System Support60 Vegetarian Caplets, Whole Food Dietary Supplement, 90…

Undeclared Soy.

Undeclared allergenView details →
Class II
FDA status: Terminated

JayRobb Vanilla Flavored Egg White Protein Powder. Net Weight 24 oz (1.5 lbs) 680g Dietary Supplement.

foreign material - plastic

Foreign materialView details →
Class III
FDA status: Terminated

ACTIRON Dietary Supplement, ActiPharma, 100 tablets (24 bottles per case) ) (Lot 13309, Exp.: 01/26)

FDA sample analysis of ACTIRON Dietary Supplement, 100 Tablets, Lot 13309, found the product did not meet folic acid specification compared to…

OtherView details →
Class I
FDA status: Terminated

Kula Can Pin¿a Colada + KRATOM SELTZER

Undeclared Allergens: Milk and Tree Nut (Coconut) and Unapproved Food Additive: Kratom

Undeclared allergenView details →
Class I
FDA status: Terminated

NUT DIET MAX, Nuez de la India, Aleurites Moluccanus, 30 Capsules, 500mg Veggie Caps

Product appears to be Yellow Oleander instead of Nuez de la India as labeled.

OtherView details →
Class II
FDA status: Terminated

100 vegetarian Fenugreek Capsules 90 count, 600mg, packaged in 150cc Amber Glass Bottle with White Polypropylene Cap.…

Foreign material: pieces of a pen (writing utensil).

Foreign materialView details →
Class II
FDA status: Terminated

100 vegetarian Fenugreek Capsules 90 count, 600mg, packaged in 150cc Amber Glass Packer with White Polypropylene Cap.

Foreign material: pieces of a pen (writing utensil).

Foreign materialView details →
Class II
FDA status: Terminated

100 vegetarian Fenugreek Capsules 90 count, 600mg, packaged in 150cc Amber Glass Packer with White Polypropylene Cap.

Foreign material: pieces of a pen (writing utensil).

Foreign materialView details →

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Same product name. Different batch. Details matter.

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