CLASS II Food recall · Reported 23 Aug 2023 · FDA Enforcement Report
Salad Kit-no Color- Lettuce-4 Way/mix-4/5# Lettuce-rom/grn recalled
NatureBest Pre-Cut & Produce is recalling Salad Kit-no Color- Lettuce-4 Way/mix-4/5# Lettuce-rom/grn Lf 60/40-4/3#, distributed in Texas. The recall was initiated on 2 Aug 2023 and the FDA has classified it as Class II.
Check your package
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-1431-2023
- FDA event ID
- 92806
- Recalling firm
- NatureBest Pre-Cut & Produce, Missouri City, TX
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 2 Aug 2023
- FDA classified
- 15 Aug 2023
- Reported
- 23 Aug 2023
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Other Reasons
- Product category
- Salad Kits
Timeline
| 2 Aug 2023 | Recall initiated by company | |
| 15 Aug 2023 | Classified by FDA | +13 days |
| 23 Aug 2023 | Published 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
Potential presence of deer fecal matter.
Product as listed by the FDA
SALAD KIT-NO COLOR-11CT LETTUCE-4 WAY/MIX-4/5# LETTUCE-ROM/GRN LF 60/40-4/3# LETTUCE-ROMAINE-SHREDDED-4/5# LETTUCE-ROM-1x1-GRN ONLY-6/2# LETTUCE-4 WAY/MIX-2/5# LETTUCE-4 WAY/MIX-1/5# LETTUCE-ROMAINE-CUT-6/2#
Where it was distributed
Texas
Questions about this recall
Why was it recalled?
Potential presence of deer fecal matter.
Which lots are affected?
190A23210, 190A23212, 190A23213-all best by dates.
Where was it sold?
Texas
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.
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