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Lower risk Food recall · FDA · Published October 27, 2021

Church Brothers True Leaf Romaine Chopped Lettuce Recall: Plastic Pieces Found

Church Brothers recalls True Leaf Romaine Chopped lettuce due to plastic pieces found in customer samples. Affected lots have use by date 10/31/21.

🇺🇸 FDA recall #F-0211-2022FoodChurch Brothers ›
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Contact the company

Recalling firmChurch Brothers, LLC19065 Portola Dr Ste C · Salinas, CA 93908-1250
✎ GovInfoNow plain-language explainer

Church Brothers is recalling True Leaf Romaine Chopped lettuce after customers found plastic pieces. This could cause injury if eaten. Consumers should check the lot code on the packaging. Read more at govinfonow.com/recall/13937-church-brothers-true-leaf-romaine-chopped-lettuce-recall-plastic-pieces.

Source Summary by GovInfoNow · govinfonow.com/recall/13937-church-brothers-true-leaf-romaine-chopped-lettuce-recall-plastic-pieces · Updated October 4, 2026 · FDA enforcement record: FDA #F-0211-2022

Cite this page

“Church Brothers True Leaf Romaine Chopped Lettuce Recall: Plastic Pieces Found.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/13937-church-brothers-true-leaf-romaine-chopped-lettuce-recall-plastic-pieces. Based on FDA recall #F-0211-2022 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0211-2022%22&limit=1).

Church Brothers, LLC voluntarily recalled True Leaf VA - Romaine Chopped due to plastic contamination, the FDA said on Oct. 27, 2021. The recall affects products distributed in Maryland.

How to tell if you have it

  • Brand: Church Brothers
  • Product: True Leaf VA - Romaine Chopped, 6x2 lb.
  • Lot Code: N288-262501-8A-11
  • Use by date: 10-31-21
  • Distribution: MD

The hazard

The FDA was notified by the FSIS of a customer finding plastic pieces in the Chopped Romaine Lettuce.

Context

GovInfoNow's records show Church Brothers, LLC had one other recall on record since Dec. 23, 2022, involving parsley contaminated with Salmonella. Other recent recalls of similar products include Ore-Ida Tater Tots Recall: Clear Plastic Fragments in Frozen Product (Dec. 3, 2025), McCain Foods Ore-Ida Tater Tots Recall: Foreign Plastic Fragments in Product (Jan. 12, 2026), and Woodstock Organic Edamame Recall: Metal Pieces Hazard (April 21, 2026).

How to tell if you have this one

Check the lot code on the packaging: N288-262501-8A-11. The product was sold in the US with a use by date of October 31, 2021.

  • Brand
    Church Brothers
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Packaging

    Look for the lot code N288-262501-8A-11 on the packaging of the True Leaf Romaine Chopped lettuce.

Where it went and when

Where it was distributed

Distributed in Maryland.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: yesMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “MD” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Maryland.

Recall timeline

FDA terminated this recall 22 days after the firm started it.

1. Firm started the recall: Oct 27, 202112. FDA classified it Class III: Nov 18, 202123. FDA terminated the recall: Nov 18, 202134. Published in FDA’s Enforcement Report: Nov 24, 202142021
  1. Firm started the recall
  2. FDA classified it Class III
  3. FDA terminated the recall
  4. Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

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Where this comes from

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-0211-2022 (October 27, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0211-2022 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.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA