Recall record at a glance
| Official record | F-0774-2018 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Bulletproof 360 Inc. |
| Report date | Feb 14, 2018 |
| Recall initiation date | Jan 23, 2018 |
| Quantity | firm reported unknown |
| Location | Seattle, WA, United States |
Official product description
Bulletproof Unflavored Collagen Protein High Performance Building Blocks Dietary Supplement, packaged in a 16-oz. composite-film bag, UPC: 8 15709 02115 3. The label is read in parts: "***COLLAGEN PROTEIN***Ingredients: Hydrolyzed collagen powder***Processed in a facility that also processes tree nuts, peanuts, egg, soy, milk, wheat, fish, crustacean shellfish***Manufactured in USA for: BULLETPROOF 360, INC. Bellevue, WA 98004***".
Why the product was recalled
Bulletproof Collagen Protein is recalled due to undeclared milk. The actual product inside the package is whey (milk) protein but mis-labeled as collagen protein.
Distribution information
distributed in CA, CO, CT, FL, GA, IA, IN, NH, NY, PA, SC, TX, WA, and WI.
How to read the classification
FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.
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.