Item FG 10149, Barlean s, Omega Man, 120 Softgels per bottle
Recalling firm: Barlean's Llc
Barlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.
Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Oct 15, 2020.
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705875100199FDA code information
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Full FDA record and distribution details
Original product description
Item FG 10149, Barlean s, Omega Man, 120 Softgels per bottle, UPC 7 05875 10019 9
Extracted codes and context
| Type | Code / value | Context |
|---|---|---|
| UPC | 705875100199 | Item FG 10149, Barlean s, Omega Man, 120 Softgels per bottle, UPC 7 05875 10019 9 |
Original FDA recall reason
Barlean's dietary supplement product is recalled due to undeclared Sulfites. Sulfite levels of finished goods does not exceed 10 ppm.
Recall details
- Recall number
- F-1367-2019
- Event ID
- 82565
- FDA status
- Terminated
- Initiated
- May 6, 2019
- Reported
- May 22, 2019
- Classified
- May 16, 2019
- Terminated
- Oct 15, 2020
- Quantity
- 1360 bottles
- Location
- Ferndale, WA, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Where it was distributed
nationwide
Data updated September 16, 2026. View official FDA data ↗
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