Class IIITerminated in FDA datasetRecall initiated May 6, 2019

Item FG 10191, Barlean s Ideal CBD Hemp Oil Softgel, 900 mg CBD, Less than 0.3% THC, 60…

Recalling firm: Barlean's Llc

Why it was recalled

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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ProductItem FG 10191, Barlean s Ideal CBD Hemp Oil Softgel, 900 mg CBD, Less than 0.3% THC, 60 Softgels per bottle. UPC 7 05875 80112 6. Item FG 10194, Barlean s Ideal CBD Hemp Oil softgel, 750 mg CBD, Less than 0.3% THC, 30 Softgels per bottle. UPC 7 05875 80114 0.
UPC705875801126, 705875801140

FDA code information

Best By of January 2021 and earlier

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Full FDA record and distribution details

Original product description

Item FG 10191, Barlean s Ideal CBD Hemp Oil Softgel, 900 mg CBD, Less than 0.3% THC, 60 Softgels per bottle. UPC 7 05875 80112 6. Item FG 10194, Barlean s Ideal CBD Hemp Oil softgel, 750 mg CBD, Less than 0.3% THC, 30 Softgels per bottle. UPC 7 05875 80114 0.

Extracted codes and context

TypeCode / valueContext
UPC705875801126D Hemp Oil Softgel, 900 mg CBD, Less than 0.3% THC, 60 Softgels per bottle. UPC 7 05875 80112 6. Item FG 10194, Barlean s Ideal CBD Hemp Oil softgel, 750 mg CBD, Less than 0.3% THC, 30 Softgels per bottle. UPC 7
UPC705875801140 Hemp Oil softgel, 750 mg CBD, Less than 0.3% THC, 30 Softgels per bottle. UPC 7 05875 80114 0.

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-1369-2019
Event ID
82565
FDA status
Terminated
Initiated
May 6, 2019
Reported
May 22, 2019
Classified
May 16, 2019
Terminated
Oct 15, 2020
Quantity
589 bottles (FG 10191); did not provide for FG 10194
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

FDA source record · F-1369-2019

Data updated September 16, 2026. View official FDA data ↗

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