ProSource Produce LLC Recall: Salmonella Oranienburg.

🇺🇸 United States

1. October 20, 2021 - Recall initiated
2. November 10, 2021 - Reported by source
3. February 18, 2022 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0111-2022

Event ID

88887

Status

Terminated

Classification

Class I

Company

ProSource Produce LLC

Product description

Whole raw RED onions are imported from Chihuahua of MEXICO. Products are packaged in 50 lb., 25 lb., 10 lb., 5 lb., 3 lb., and 2 lb. mesh sacks and in 50 lb., 40 lb., 25 lb., 10 lb., and 5 lb. cartons. Products are distributed and/or sold under the brands Big Bull, Markon First Crop, Markon Essentials, Peak Fresh Produce, Rio Blue, Rio Valley, ProSource, Sierra Madre, and Sysco Imperial Fresh.

Quantity

6,820,172 lbs.

Reason

Salmonella Oranienburg.

Recall initiation date

October 20, 2021

Report date

November 10, 2021

Classification date

Not published in this source record

Termination date

February 18, 2022

Distribution pattern

Distributed in AL, AR, AZ, CA, CO, CT, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, NC, NE, NJ, NM, NY, OH, OK, PA, RI, SC, TN, TX, VA, and WI, as well as Ontario and Quebec, Canada.

UPC, lot, and code information

Lot Codes for all RED whole onions: 325 1102 1103 1125 1126 1127 1232 2141127 AB161ORRL183 ABA131ORR158 ABALS1ORR155 ABL161ORR155 ABL161ORR158 ABL161ORS153 ABL161ORS154 AGC261ORRL183 AGC261ORRL184 AGC261ORRL187 AGCEA11OR6005209 AGCRVF41ORM195 AGUL11OR6005180 AGUL11OR6005181 AGUL11OR6005183 AGUL11OR6005186 AGUL11OR6005187 APL171ORR158 APL171ORRL195 APL171ORRL205 APL171ORS159 APL31OR6005180 APL31ORMO183 APL31ORS165 APL51OR6005181 APL51OR6005182 APL51ORMO182 ASM191ORR144 CBK21ORM168 CBKL210RM159 CBKL21ORM160 CRC26RRL CRRV16RRL CRRVF16RMA CRRVF17RMA CRRVF19R05 CRRVF3R05 CRRVF4RMO EMT111ORM218 GR841OR6005186 GR841OR6005193 GR841OR6005195 GR841OR6005196 GR91ORRL195 GRL41OYRM167 IGV211OR6005196 JAB1901ORR158 JGN101ORM173 JGN121ORM172 JHW431ORMO201 JHW431ORMO203 JHW431ORMO204 JHW431ORMO207 JHW431ORMO209 JHW431ORMO210 JHW431ORRL200 JKP051OR6005196 JKP51ORRL187 JKP51ORRL189 JKP61ORRL182 JKP61ORRL186 JKPL211ORS154 JWW11710RRL217 JWW1171ORRL218 LR4RRR LR5RRT LRRN4RMO LRRN7RRL LRRV10R05 LRRV8RRL RMKRN41ORRL203 RMKRN61ORRL211 TYJ4M31ORM167 TYJ4M31ORM168 TYJ4M31ORM169 TYJ4M61ORM173 TYJ4M61ORM193 TYJ4M61ORMO183 TYJ4M61ORMO188 TYJ4M61ORR160 TYJ4M61ORRL180 TYJ4M61ORRL181 TYJ4M61ORRL186 TYJ4M61ORRL187 TYJ61ORM194 TYJ61ORMO197 TYJ61ORMO198 TYJ61ORMO201 TYJ61ORMO202 TYJ61ORMO203 VBJHRMO

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Press Release

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Other products recalled under this same event

This recall shares FDA event ID 88887 with 2 other product entries in Public Health Trace.

Responsible company: ProSource Produce LLC

Other recalls from ProSource Produce LLC

A map highlighting the states named in the source's distribution description.

Distributed No data published

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map

State	Distributed
Alabama	1
Arkansas	1
Arizona	1
California	1
Colorado	1
Connecticut	1
Florida	1
Georgia	1
Iowa	1
Idaho	1
Illinois	1
Indiana	1
Kansas	1
Kentucky	1
Louisiana	1
Massachusetts	1
Maryland	1
Michigan	1
Minnesota	1
Missouri	1
Mississippi	1
North Carolina	1
Nebraska	1
New Jersey	1
New Mexico	1
New York	1
Ohio	1
Oklahoma	1
Pennsylvania	1
Rhode Island	1
South Carolina	1
Tennessee	1
Texas	1
Virginia	1
Wisconsin	1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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