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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 48 of 110
Class II
FDA status: Terminated

Polyvitamin 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

Tri-Vitamin, 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

Liquid Vitamin C

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

Other contaminationView details →
Class II
FDA status: Terminated

CertaVite with Antioxidants

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

Other contaminationView details →
Class II
FDA status: Terminated

Poly-Vita Drops, 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

Poly-Vita Drops 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 →
Class II
FDA status: Terminated

D-Vita Drops, 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

Ferrous Drops, 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

Tri-Vita Drops, 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

Pedia Tri-Vite Drops, 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

Pedia Tri-Vite Drops 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 →
Class II
FDA status: Terminated

Pedia Poly-Vite Drops, 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 →

Found your product? Now check the codes.

Same product name. Different batch. Details matter.

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