CLASS III Food recall · Reported 24 Nov 2021 · FDA Enforcement Report

True Leaf VA - Romaine Chopped, lb. True Leaf recalled

Church Brothers is recalling True Leaf VA - Romaine Chopped, lb. True Leaf, distributed in Maryland. The recall was initiated on 27 Oct 2021 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codesLot Code N288-262501-8A-11 Use by 10-31-21
Quantity recalled90 cases

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0211-2022
FDA event ID
88942
Recalling firm
Church Brothers, Salinas, CA
Classification
Class III
Status
Terminated
Recall initiated
27 Oct 2021
FDA classified
18 Nov 2021
Reported
24 Nov 2021
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Foreign Material
Product category
Romaine Lettuce

Timeline

27 Oct 2021Recall initiated by company
18 Nov 2021Classified by FDA+22 days
24 Nov 2021Published in enforcement report+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

FSIS notified FDA of a customer finding plastic pieces in Chopped Romaine Lettuce

Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.

Product as listed by the FDA

True Leaf VA - Romaine Chopped, 6x2 lb. True Leaf Product of USA

Where it was distributed

MD

Maryland

Questions about this recall

Why was it recalled?

FSIS notified FDA of a customer finding plastic pieces in Chopped Romaine Lettuce

Which lots are affected?

Lot Code N288-262501-8A-11 Use by 10-31-21

Where was it sold?

MD

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class III mean?

Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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