CLASS I Food recall · Reported 2 Sep 2015 · FDA Enforcement Report

Caesar Salad, #5.56 "Ingredients: Romaine Lettuce recalled

Fresh Unlimited is recalling Caesar Salad, #5.56 "Ingredients: Romaine Lettuce, Caesar Dressing (Soybean oil, water, distributed in Indiana, Kentucky, Massachusetts, Ohio, Pennsylvania. The recall was initiated on 8 Jul 2015 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesProduct #74810 TC 11741319 BEST USED BY: 7/6/15, TC 11751319 BEST USED BY: 7/5/15, TC 11761319 BEST USED BY: 7/8/15, TC 11771319 BEST USED BY: 7/9/15, TC 11801319 BEST USED BY: 7/12/15, TC 11811319 BEST USED BY: 7/12/15, TC 11821319 BEST USED BY: 7/13/15, TC 11822319 BEST USED BY: 7/13/15, TC 11831319 BEST USED BY: 7/13/15 & 7/14/15, TC 11871319 BEST USED BY: 7/17/15.
Quantity recalled829/5.56# kits/box

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-3051-2015
FDA event ID
71683
Recalling firm
Fresh Unlimited, Sidney, OH
Brand
Caesar
Classification
Class I
Status
Terminated
Recall initiated
8 Jul 2015
FDA classified
24 Aug 2015
Reported
2 Sep 2015
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Undeclared Egg
Product category
Salad Kits

Timeline

8 Jul 2015Recall initiated by company
24 Aug 2015Classified by FDA+47 days
2 Sep 2015Published in enforcement report+9 days

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

Reason for recall

The firm failed to declare the allergen eggs on their labels.

Product as listed by the FDA

Caesar Salad, #5.56 (2,522g) "INGREDIENTS: Romaine Lettuce, Caesar Dressing (Soybean oil, water, distilled vinegar, Romano cheese (pasteurized part skim milk, cheese culture, salt, enzymes),*****" *ALLERGENS** Fish, Milk, Wheat

Where it was distributed

Product was shipped to the following states: IN, KY, MA, OH & PA.

IndianaKentuckyMassachusettsOhioPennsylvania

Questions about this recall

Why was it recalled?

The firm failed to declare the allergen eggs on their labels.

Which lots are affected?

Product #74810 TC 11741319 BEST USED BY: 7/6/15, TC 11751319 BEST USED BY: 7/5/15, TC 11761319 BEST USED BY: 7/8/15, TC 11771319 BEST USED BY: 7/9/15, TC 11801319 BEST USED BY: 7/12/15, TC 11811319 BEST USED BY: 7/12/15, TC 11821319 BEST USED BY: 7/13/15, TC 11822319 BEST USED BY: 7/13/15, TC 11831319 BEST USED BY: 7/13/15 & 7/14/15, TC 11871319 BEST USED BY: 7/17/15.

Where was it sold?

Product was shipped to the following states: IN, KY, MA, OH & PA.

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.

Other products in this recall event

2 other products · FDA event 71683

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