CLASS I Food recall · Reported 6 Dec 2023 · FDA Enforcement Report

GreenGate Fresh Standard Cello Spinach recalled

GreenGate Fresh LL is recalling GreenGate Fresh Standard Cello Spinach, distributed in 7 states. The recall was initiated on 10 Nov 2023 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesBag Codes: 313 SB7 465, 313 SB8 465; Case codes: SB7 23 313, SB8 23 313
Quantity recalled11 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-0480-2024
FDA event ID
93421
Recalling firm
GreenGate Fresh LL, Salinas, CA
Classification
Class I
Status
Terminated
Recall initiated
10 Nov 2023
FDA classified
29 Nov 2023
Reported
6 Dec 2023
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
E. coli
Product category
Lettuce

Timeline

10 Nov 2023Recall initiated by company
29 Nov 2023Classified by FDA+19 days
6 Dec 2023Published in enforcement report+7 days

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

Reason for recall

Potential E. coli (EHEC) contamination

Some strains of E. coli, such as O157:H7, produce a toxin that can cause severe stomach cramps, bloody diarrhea and, in a small number of cases, kidney failure.

Product as listed by the FDA

GreenGate Fresh Standard Cello Spinach; 4 - 2.5lb plastic bags per box; SKU 465; Perishable hence require refrigeration at all times of its shelflife

Where it was distributed

Total number of consignees that received the recall product: 8. Total number of distributors that received the recall product: 8. Recalled product distributed in the following U.S. states: SC, IL, MO, MA, TX, CA, MI.

CaliforniaIllinoisMassachusettsMichiganMissouriSouth CarolinaTexas

Questions about this recall

Why was it recalled?

Potential E. coli (EHEC) contamination

Which lots are affected?

Bag Codes: 313 SB7 465, 313 SB8 465; Case codes: SB7 23 313, SB8 23 313

Where was it sold?

Total number of consignees that received the recall product: 8. Total number of distributors that received the recall product: 8. Recalled product distributed in the following U.S. states: SC, IL, MO, MA, TX, CA, MI.

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 I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

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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