Recall record at a glance
| Official record | F-0181-2022 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Bix Produce Company LLC |
| Report date | Nov 24, 2021 |
| Recall initiation date | Oct 21, 2021 |
| Quantity | 27,445 lbs. |
| Location | Saint Paul, MN, United States |
Official product description
Raw onion sold in bags or sliced and diced with the following item numbers and lot code. 1. RED JUMBO 25# 1/25 LB, item 06370; 2. ONIONS,RED JUMBO 1/5 LB, item 06373; 3. ONIONS,RED MEDIUM 1/25 LB, item 06380; 4. ONIONS,WHITE JUMBO 50# 1/50 LB, item 06430; 5. ONIONS,WHITE JUMBO 25# 1/25 LB, item 06431; 6. ONIONS,WHITE JUMBO 1/10 LB, item 06433; 7. ONIONS,YELLOW JUMBO N&DE 1/50 LB, item 06439; 8. ONIONS,YELLOW JUMBO 50# 1/50 LB, item 06450; 9. ONIONS,YELLOW JUMBO 25# 1/25 LB, Item 06452; 10. ONIONS,YELOW JUMBO 1/10 LB, item 06453; 11. ONION,WHITE DICED 3/8" 1/5 LB, item 13730; 12. ONION,WHITE DICED 1/2" 1/5 LB, item 13731; 13. ONION,WHITE DICED 1/4" 1/20 LB, item 13733; 14. ONION,WHITE DICED 1/8" 1/5 LB, item 13734; 15. ONION,WHITE JULIENNE 1/8" 1/5 lb, item 13735; 16. ONION,WHITE JULIENNE 1/4" 1/5 LB, Item 13736; 17. ONION,WHITE WHOLE PEELED 1/10 LB, item 13738; 18. ONION,WHITE SLICED 1/8" 1/5 LB, item 13745; 19. ONION,WHITE SLICE 1/4" 1/5 LB, item 13750; 20. ONION,WHITE SLICED 1/4" 4/5 LB, item 13751; 21. ONION RED JUMBO 50# TCFI 1/50 LB, item 25034.
Why the product was recalled
Onions may be contaminated with Salmonella
Distribution information
IA, MN, ND, SD, 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: Telephone.
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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