CLASS I Food recall · Reported 8 Jan 2020 · FDA Enforcement Report

Company's Honey Bear Small Party Platter recalled

Mrs. Condies Salad is recalling Company's Honey Bear Small Party Platter containing Ranch Dressing dip, distributed in Colorado. The recall was initiated on 3 Dec 2019 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesBEST BY 12/9/19 (10 days from manufacture).
Quantity recalled6 trays

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-0449-2020
FDA event ID
84457
Recalling firm
Mrs. Condies Salad, Denver, CO
Classification
Class I
Status
Terminated
Recall initiated
3 Dec 2019
FDA classified
31 Dec 2019
Reported
8 Jan 2020
Type
Voluntary: Firm initiated
Customers notified by
Telephone
Reason category
Undeclared Milk
Product category
Salad Kits

Timeline

3 Dec 2019Recall initiated by company
31 Dec 2019Classified by FDA+28 days
8 Jan 2020Published 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

Ranch Dressing dip contains undeclared milk as an ingredient.

Product as listed by the FDA

Mrs. Condies Salad Company's Honey Bear Small Party Platter containing Ranch Dressing dip,3.5 lbs.

Where it was distributed

Castle Pines, CO

Colorado

Questions about this recall

Why was it recalled?

Ranch Dressing dip contains undeclared milk as an ingredient.

Which lots are affected?

BEST BY 12/9/19 (10 days from manufacture).

Where was it sold?

Castle Pines, CO

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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