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Dietary supplements Recalls

Are there any current dietary supplements recalls?

24 recent FDA-listed ongoing recall records in this snapshot.FDA data updated September 16, 2026 · Snapshot assessed September 18, 2026
View recent ongoing records →

“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 34 of 110
Class III
FDA status: Terminated

Item FG 10089, Barlean s, Fish Oil Omega-3 EPA/DHA Orange Flavor, 100 Softgels per bottle.

Barlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.

Undeclared allergenView details →
Class III
FDA status: Terminated

Item FG 10106, Barlean s, Olive Leaf Complex, 120 Softgels per bottle.

Barlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.

Undeclared allergenView details →
Class III
FDA status: Terminated

Item FG 10116, Barlean s, Master Blend Total Omega 3.6.9 Lemonade Flavor, 90 Softgels per bottle.

Barlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.

Undeclared allergenView details →
Class III
FDA status: Terminated

Item FG 10146, Barlean s, Essential Woman

Barlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.

Undeclared allergenView details →
Class III
FDA status: Terminated

Item FG 10149, Barlean s, Omega Man, 120 Softgels per bottle

Barlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.

Undeclared allergenView details →
Class III
FDA status: Terminated

Item FG 10190, Barleans Full Spectrum Hemp Extract, 60 Softgels per bottle.

Barlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.

Undeclared allergenView details →
Class III
FDA status: Terminated

Item FG 10191, Barlean s Ideal CBD Hemp Oil Softgel, 900 mg CBD, Less than 0.3% THC, 60 Softgels per bottle.

Barlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.

Undeclared allergenView details →
Class III
FDA status: Terminated

Item FG 10079, Barleans, Flax Oil, 100 Softgels per bottle.

Barlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.

Undeclared allergenView details →
Class I
FDA status: Terminated

Life Rising Holder-W Holder Warmer capsules

High lead levels in products

Lead / heavy metalsView details →
Class II
FDA status: Terminated

Life Rising NECK-ND Neck Clear capsules

High lead levels in products

Lead / heavy metalsView details →
Class II
FDA status: Terminated

Dried whole elderberry, Oregon s Wild Harvest brand, packaged in metalized plastic bag, net wt. 4 oz or 1 lb. Each case…

Dried whole Elderberries are recalled due to glass fragments contamination.

Foreign materialView details →
Class II
FDA status: Terminated

Addback Tablet Dietary Supplement 60 tablets per 190cc Oblong WHDPE bottle Net Wet: 85gm (60 tablet wt)

Undeclared coating ingredients: HPMC, Triacetin, Titanium Dioxide, FD & C Yellow # 5, FD & C Yellow # 6, FD & C Blue # 1. In addition, the label…

Labeling / mislabelingView details →

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Same product name. Different batch. Details matter.

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