FDA recall record

Bulletproof Digital FATwater bottle, 16.9 fl recall — FDA F-0576-2016

FATwater bottles, Lemon flavor, are recalled due to microbial growth detection. No E.coli or other pathogens were detected.

Class IIIclassification
F-0576-2016official record ID
Feb 17, 2016report date

Recall record at a glance

Official recordF-0576-2016
CategoryFood Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmBulletproof Digital Inc.
Report dateFeb 17, 2016
Recall initiation dateDec 10, 2015
Quantity12,776 bottles
LocationBellevue, WA, United States

Official product description

FATwater bottle, 16.9 fl. oz., Lemon flavor, UPC 6 09015 50475 8

Why the product was recalled

FATwater bottles, Lemon flavor, are recalled due to microbial growth detection. No E.coli or other pathogens were detected.

Distribution information

distributed in CA, OR, and TX. Products sold from bulletproof.com to internet customers nationwide and Canada.

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement 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

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

Related recall records

Other records from the same recalling company are shown first when available.