CLASS I Food recall · Reported 19 Mar 2025 · FDA Enforcement Report
Southwest Salad Kit recalled by Little Leaf Farms
Little Leaf Farms is recalling Southwest Salad Kit, distributed in Connecticut, Massachusetts, New Hampshire. The recall was initiated on 28 Feb 2025 and the FDA has classified it as Class I.
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-0637-2025
- FDA event ID
- 96409
- Recalling firm
- Little Leaf Farms, Shirley, MA
- Brand
- Little Leaf
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 28 Feb 2025
- FDA classified
- 13 Mar 2025
- Reported
- 19 Mar 2025
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Undeclared Wheat & Gluten
- Product category
- Salad Kits
Timeline
| 28 Feb 2025 | Recall initiated by company | |
| 13 Mar 2025 | Classified by FDA | +13 days |
| 19 Mar 2025 | Published 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
Product may contain incorrect salad dressing, resulting in fish and wheat being undeclared.
Product as listed by the FDA
Little Leaf Farms brand Southwest Salad Kit; 7.5 oz, clear plastic clamshell; UPC: 857394006220
Where it was distributed
MA, NH, CT
Questions about this recall
Why was it recalled?
Product may contain incorrect salad dressing, resulting in fish and wheat being undeclared.
Which lots are affected?
Lot Number: 050011; Enjoy by: 3/08/2025
Where was it sold?
MA, NH, CT
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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