FDA recall record

Threshold Enterprises Planetary Herbals Ginseng Classic recall — FDA F-3338-2017

Product was inadvertently released prior to release of all QC testing. Testing had positive results for coliform growth.

Class IIclassification
F-3338-2017official record ID
Aug 9, 2017report date

Recall record at a glance

Official recordF-3338-2017
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmThreshold Enterprises Ltd
Report dateAug 9, 2017
Recall initiation dateJun 16, 2017
Quantity36 bottles - 7 x 120 count and 29 x 60 count.
LocationScotts Valley, CA, United States

Official product description

Planetary Herbals Ginseng Classic; Classic Chinese Energizer 710 mg; 60 and 120 UPC 0 21078 10215 1 tablet bottles; 60 count - UPC 0 21078 10214 4; Product code PF0214 120 count - UPC 0 21078 10215; Product code PR0215.

Why the product was recalled

Product was inadvertently released prior to release of all QC testing. Testing had positive results for coliform growth.

Distribution information

CA, MN, WA, IL, PR, ME, SD.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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