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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

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

1,310 recall recordsPage 47 of 110
Class I
FDA status: Terminated

Dietary Supplement Acidophilus Blend, 90 capsules, Product No. E-420, packaged in 225cc HDPE white bottle, room temp,…

Nature's Power Solutions Acidophilus Blend due to undeclared milk allergen.

Undeclared allergenView details →
Class II
FDA status: Terminated

SYNEDREX, Powerful stimulant weight loss solution, 45 capsules (

Products contain Picamilon and/or methylpentane citrate (DMBA), which are not recognized as a dietary ingredients

OtherView details →
Class II
FDA status: Terminated

CANNIBAL RIOT, SUPER STIMULANT PRE-WORKOUT ENERGY COMPLEX, FIVE FINGER DEATH PUNCH, Chaos and Pain, DIETARY…

The products are being recalled because they contain 750 mg of Agmatine and 50 mg 1,3 Dimethylbutylamine per serving which is not declared on…

Labeling / mislabelingView details →
Class II
FDA status: Terminated

CANNIBAL RIOT, SUPER STIMULANT PRE-WORKOUT ENERGY COMPLEX, UNICORN BLOOD, Chaos and Pain, DIETARY SUPPLEMENTS, NET.WT.…

The products are being recalled because they contain 750 mg of Agmatine and 50 mg 1,3 Dimethylbutylamine per serving which is not declared on…

Labeling / mislabelingView details →
Class II
FDA status: Terminated

Virtrate-2, Sodium Citrate-Citric Acid, 16oz./473 mL, OTC Non-Sterile. Dietary supplement.

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

Other contaminationView details →
Class II
FDA status: Terminated

Virtrate-K, Potassium Citrate and Citric Acid, 16oz./473 mL, OTC Non-Sterile. Dietary supplement.

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

Other contaminationView details →
Class II
FDA status: Terminated

Calcionate Syrup, Calcium Glubionate Syrup

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

Other contaminationView details →
Class II
FDA status: Terminated

D3 Vitamin Liquid, 50 mL, OTC Non-Sterile. Dietary supplement.

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

Other contaminationView details →
Class II
FDA status: Terminated

Cerovite Liquid

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

Other contaminationView details →
Class II
FDA status: Terminated

Ferrous Sulfate Liquid

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

Other contaminationView details →
Class II
FDA status: Terminated

Fer-Iron Liquid, 50 mL, OTC Non-Sterile. Dietary supplement.

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

Other contaminationView details →
Class II
FDA status: Terminated

Polyvitamin Liquid with Iron, 50 mL, OTC Non-Sterile. Dietary supplement.

Recall initiated as a precautionary measure due to potential risk of product contamination with Burkholderia cepacia.

Other contaminationView details →

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Same product name. Different batch. Details matter.

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