CLASS III Food recall · Reported 22 May 2019 · FDA Enforcement Report

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

Barlean's is recalling Item FG 10149, Barlean s, Omega Man, 120 Softgels per bottle, distributed nationwide in the US. The recall was initiated on 6 May 2019 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codesBest By of January 2022 and earlier
Quantity recalled1360 bottles

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-1367-2019
FDA event ID
82565
Recalling firm
Barlean's, Ferndale, WA
Brand
Item FG
Classification
Class III
Status
Terminated
Recall initiated
6 May 2019
FDA classified
16 May 2019
Reported
22 May 2019
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Undeclared Sulfites
Product category
Dietary Supplements

Timeline

6 May 2019Recall initiated by company
16 May 2019Classified by FDA+10 days
22 May 2019Published in enforcement report+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

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

Product as listed by the FDA

Item FG 10149, Barlean s, Omega Man, 120 Softgels per bottle, UPC 7 05875 10019 9

Where it was distributed

nationwide

Nationwide

Questions about this recall

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

Yes. Barlean's recalled Item FG 10149, Barlean s, Omega Man, 120 Softgels per bottle on 6 May 2019. The recall is Class III and its status is Terminated. Recall number F-1367-2019.

Why was it recalled?

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

Which lots are affected?

Best By of January 2022 and earlier

Where was it sold?

nationwide

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class III mean?

Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

More recalls from Barlean's

All 12
ReportedClassRecallCompanyReasonWhere
FoodCLASS IIIItem FG 10116, Barlean s, Master Blend Total Omega 3.6.9 Lemonade recalledItem FGBarlean'sUndeclared SulfitesNationwide
FoodCLASS IIIItem FG 10191, Barlean s Ideal CBD Hemp Oil Softgel recalledItem FGBarlean'sUndeclared SulfitesNationwide
FoodCLASS IIIItem FG 10089, Barlean s, Fish Oil Omega-3 EPA/DHA Orange recalledItem FGBarlean'sUndeclared SulfitesNationwide
FoodCLASS IIIItem FG 10190, Barleans Full Spectrum Hemp Extract, 60 Softgels recalledItem FGBarlean'sUndeclared SulfitesNationwide
FoodCLASS IIIItem FG 10106, Barlean s, Olive Leaf Complex recalledItem FGBarlean'sUndeclared SulfitesNationwide

Other Dietary Supplements recalls

All 733
ReportedClassRecallCompanyReasonWhere
FoodANNOUNCEDNiwali Tejocote Capsules and Pieces recalled by Global MixNiwaliGlobal MixForeign MaterialNationwide
FoodCLASS IAddall XR Shot, liquid dietary supplement recalled by ZMB EnterprisesAddall XRZMB EnterprisesHidden Drug IngredientsCA
FoodCLASS IISuper Skin; Dietary Supplement;, 2 per day recalled by Mellish IslandMellish IslandMellish IslandOtherNationwide
FoodCLASS IModern Warrior Ready, Dietary Supplement recalledModern WarriorModern Warrior LifeHidden Drug IngredientsNationwide
FoodCLASS IIVista MAX; Dietary Supplement Serving Size recalled by Provision HealthVista MAXProvision HealthUndeclared AllergensCA