“Church Brothers Parsley Bunches Contaminated with Salmonella - Recall.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/12035-church-brothers-parsley-bunches-contaminated-with-salmonella-recall. Based on FDA recall #F-0310-2023 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0310-2023%22&limit=1).
The FDA announced on Dec. 23, 2022, that Church Brothers, LLC voluntarily recalled parsley bunches due to Salmonella contamination risks. The Class I recall affects product distributed to Louisiana, Florida, and Michigan.
How to tell if you have it
Brand: Church Brothers
Product: Parsley bunches Boxes of 30 and 60 count Keep refrigerated SKU 475987 PLU 4899 on twist ties Product of Mexico
GS1 Lot: CB229534
Quantity: 327 cases
The hazard
Parsley imported from Mexico was found to be contaminated with Salmonella, according to the FDA. The agency classified this as a Class I recall.
Context
GovInfoNow's records show Church Brothers, LLC has one other recall on record since Oct. 27, 2021, involving plastic pieces in chopped romaine lettuce. Other recent recalls of similar products include Pacific Italian Parsley Bags Recall (Oct. 27, 2025), Solina Parmesan Breadstick Sauce Seasoning Recall (April 24, 2026), and JCB Flavors Butter Parsley Recall (May 1, 2026).
How to tell if you have this one
Check for parsley bunches in boxes of 30 or 60 count with SKU 475987 and PLU 4899 on twist ties. Products were imported from Mexico and labeled with GS1 Lot: CB229534.
Brand
Church Brothers
Category
Food
Based on the official FDA remedy
What to do — step by step
Stop Using Now
Immediately stop using and discard any parsley bunches with SKU 475987 and PLU 4899 on twist ties.
Where it went and when
Where it was distributed
Distributed in 3 states.
Listed by the agency
Not listed
FDA distribution: “Product was distributed to LA, FL, and MI” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Florida, Louisiana, Michigan.
Recall timeline
FDA terminated this recall 32 days after the firm started it.
1Firm started the recall
2FDA classified it Class I
3FDA terminated the recall
4Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #F-0310-2023 (December 23, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0310-2023 to see it in context.
Plain-language summary written by qwen3:4b on October 4, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.