CLASS II ONGOING Food recall · Reported 23 Aug 2023 · FDA Enforcement Report

Lettuce Mix w 20 Romaine, Produce recalled by G.O

G.O is recalling Lettuce Mix w 20 Romaine, Produce, distributed in Iowa, Minnesota, North Dakota, Wisconsin. The recall was initiated on 1 Aug 2023 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot Code: 130212
Quantity recalled23,186 lbs. total

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-1426-2023
FDA event ID
92828
Recalling firm
G.O, Minneapolis, MN
Classification
Class II
Status
Ongoing
Recall initiated
1 Aug 2023
FDA classified
15 Aug 2023
Reported
23 Aug 2023
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Other Reasons
Product category
Fish

Timeline

1 Aug 2023Recall initiated by company
15 Aug 2023Classified by FDA+14 days
23 Aug 2023Published in enforcement report+8 days

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

Reason for recall

Romaine lettuce may be contaminated with deer feces.

Product as listed by the FDA

Lettuce Mix w 20 Romaine, Produce Code 421009, 4-5 lb. bags per shipping case,

Where it was distributed

IA, MN, ND, WI

IowaMinnesotaNorth DakotaWisconsin

Questions about this recall

Why was it recalled?

Romaine lettuce may be contaminated with deer feces.

Which lots are affected?

Lot Code: 130212

Where was it sold?

IA, MN, ND, WI

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 II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

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.

Other products in this recall event

7 other products · FDA event 92828

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