CLASS I Food recall · Reported 18 Jul 2018 · FDA Enforcement Report

Wish Bone House Italian Salad Dressing recalled by Pinnacle Food Group

Pinnacle Food Group is recalling Wish Bone House Italian Salad Dressing, distributed nationwide in the US. The recall was initiated on 28 Jun 2018 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesItem number 004132100648 Case Lot Code 4913019S51
Quantity recalled7,768 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-1655-2018
FDA event ID
80405
Recalling firm
Pinnacle Food Group, Cherry Hill, NJ
Classification
Class I
Status
Terminated
Recall initiated
28 Jun 2018
FDA classified
19 Jul 2018
Reported
18 Jul 2018
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Undeclared Milk
Product category
Salad Kits

Timeline

28 Jun 2018Recall initiated by company
18 Jul 2018Published in enforcement report+20 days
19 Jul 2018Classified by FDA+1 day

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

Reason for recall

The recall was initiated after learning from a retail customer that a limited number of bottles were mislabeled. The product contains milk and egg not declared on the bottle.

Product as listed by the FDA

Wish Bone House Italian Salad Dressing 15 oz.

Where it was distributed

73 locations received the product. The locations are a mix of retailers and distributors. Product was distributed nationwide to receiving locations in 31 states.

Nationwide

Questions about this recall

Why was it recalled?

The recall was initiated after learning from a retail customer that a limited number of bottles were mislabeled. The product contains milk and egg not declared on the bottle.

Which lots are affected?

Item number 004132100648 Case Lot Code 4913019S51

Where was it sold?

73 locations received the product. The locations are a mix of retailers and distributors. Product was distributed nationwide to receiving locations in 31 states.

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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