CLASS I Food recall · Reported 26 Nov 2014 · FDA Enforcement Report

Wawa Garden Rotini Salad with Lite Creamy Caesar Dressing recalled

Taylor Farms New Jersey NJ is recalling Wawa Garden Rotini Salad with Lite Creamy Caesar Dressing, distributed in Maryland, New Jersey, Pennsylvania. The recall was initiated on 2 Nov 2014 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codessell by 11/04/2014 TFNJ 303 1 5:00am
Quantity recalled1,510 units

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-0529-2015
FDA event ID
69661
Recalling firm
Taylor Farms New Jersey NJ, Swedesboro, NJ
Classification
Class I
Status
Terminated
Recall initiated
2 Nov 2014
FDA classified
20 Nov 2014
Reported
26 Nov 2014
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Product category
Salad Kits

Timeline

2 Nov 2014Recall initiated by company
20 Nov 2014Classified by FDA+18 days
26 Nov 2014Published 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 recalled due to the potential of undeclared fish, wheat and egg allergens.

Product as listed by the FDA

Wawa Garden Rotini Salad with Lite Creamy Caesar Dressing, Net Wt 8 oz. (227 g) Bottom of container - Wawa Kale & Quinoa Salad Distributed by: Wawa, Inc. Wawa, PA 19063 UPC 726191066402

Where it was distributed

MD, PA & NJ

MarylandNew JerseyPennsylvania

Questions about this recall

Why was it recalled?

Product recalled due to the potential of undeclared fish, wheat and egg allergens.

Which lots are affected?

sell by 11/04/2014 TFNJ 303 1 5:00am

Where was it sold?

MD, PA & NJ

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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