Raw onion sold in bags or sliced and diced with the following item numbers and lot code. 1. RED JUMBO 25# 1/25 LB, it... — FDA record F-0181-2022

Reported terminated

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Oct 21, 2021. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.

What the record says

Product
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.
Reason
Onions may be contaminated with Salmonella
Classification
Class I
Recalling firm
Bix Produce Company LLC
Quantity
27,445 lbs.
Agency-reported status
Terminated
Source record identifier
F-0181-2022

Open the official record

What the recall classes mean. Classification is an agency assessment, not individual medical advice.

Lot and product identifiers

Label fieldDetails supplied by the agency
Lot, code or applicabilityLot Codes: 1. 19322501 2. P2206554-00 3. 19322501-00, and 19322501-01 4. 19222803, 19257101, and 19322502 5. 19222803-00, 19222803-01, and 19257101-00 6. P2192841-00, P2193814-00 7. 19322503-00 8. 19259005, 19268601, 19294705, 19315301 9. P4091750-00 10. P2208659-00, P2208659-00, P2218562-00 11. P2190993-00, P2192357-00, P2193277-00, P2203169-00, and P2204976-00 12. P2189276-00, P2190950-00, P2192188-00, P2194082-00, P2204086-00, P2204966-00 13. P2190917-00, P2192239-00, P2194072-00 14. P2203143-00, P2205094-00 15. P2192216-00 16. P2194150-00, P2204087-00 17. P2193462-00 18. P2191022-00, P2191201-00, P2192379-00, P2205040-00 19. P2191119-00, P2193740-00 20. P2190938-00, P2191982-00, P2192252-00, P2194153-00 21. 19322501-00

Match all identifying details in the current notice. A brand name alone is not enough.

Distribution

IA, MN, ND, SD, WI

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

Dates in the source

Report date
Nov 24, 2021
Recall initiation date
Oct 21, 2021
Center classification date
Nov 17, 2021
Termination date
Dec 8, 2021

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

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