Recall record at a glance
| Official record | F-2182-2017 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | BEYOND MEAT |
| Report date | May 10, 2017 |
| Recall initiation date | Apr 13, 2017 |
| Quantity | 4665 cases (3856 retail packages/8366 food service packages) |
| Location | El Segundo, CA, United States |
Official product description
Beyond Beef Feisty Crumble Vegan Gluten-free Non-GMO Weight: 10 lbs. (2) 5 lb. bags UPC: 10852629004412 KEEP FROZEN 111 Main Street El Segundo, CA 90245 866-756-4112 customer@beyondmeat.com www.beyondmeat.com; Beyond Meat Beyond Beef Crumbles Feisty Net WT 11oz (312g) KEEP FROZEN Plant Based Protein Crumbles UPC: 852629004132
Why the product was recalled
Undeclared peanuts
Distribution information
CA, FL, MO, IL
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.