CLASS II Food recall · Reported 28 Sep 2022 · FDA Enforcement Report

Triple Berry Parfait recalled by Russ Davis Wholesale

Russ Davis Wholesale is recalling Triple Berry Parfait, distributed in Iowa, Michigan, Minnesota, North Dakota, South Dakota, Wisconsin. The recall was initiated on 29 Jul 2022 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codes1. Lot Code: X5950748, X5950748, X5955610, X5950748, X5955610, X5957211, X5955610, X5955610, X5957211, X5960185, X5955610, X5960185, X5961784, X5960185, X5961784, X5965071, X5961784, X5965071, X5967083, X5965071, X5967083, X5970251, X5967083, X5970251, X5973394, X5970251, X5973394, X5976408, X5978626, X5973394, X5976408, X5978626, X5976408, X5978626, X5981915, X5978626, X5981915, X5984747, X5981915, X5984747, X5987204, X5984747, X5987204, X5990635, X5987204, X5990635, X5993277, X5990635, X5993277, X5996223, X5993277, X5996223, X5998844, X5996223, X5998844. Use by Dates: 7/13-8/3/2022 2. Lot Code: X5953078, X5956997, X5959085, X5962068, X5967308, X5964566, X5967308, X5969823, X5973066, X5975958, X5978859, X5981505, X5984210, X5986763, X5990384, X5992845, X5995680, X5998398, X6001019. Use by Dates: 7/13-8/3/2022
Quantity recalled87,915 units total

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-1757-2022
FDA event ID
90694
Recalling firm
Russ Davis Wholesale, Inver Grove Heights, MN
Classification
Class II
Status
Terminated
Recall initiated
29 Jul 2022
FDA classified
22 Sep 2022
Reported
28 Sep 2022
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Packaging Defects
Product category
Other

Timeline

29 Jul 2022Recall initiated by company
22 Sep 2022Classified by FDA+55 days
28 Sep 2022Published 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

Various vegetable and fruit products are recalled due to inadequate sanitizer in wash water.

Packaging recalls include wrong labels, wrong products in the wrong bottle, missing leaflets, short-filled or empty capsules and seals that fail.

Product as listed by the FDA

Triple Berry Parfait, Net Wt. 6 oz (170 g) Keep Refrigerated. Packaged under the following brands: 1. Item 80732 Crazy Fresh, or quick & easy. UPC 95631-80732 2. Item 80737 Kowalski's Markets. UPC 95631-80737

Where it was distributed

IA, MI, MN, ND, SD, WI

IowaMichiganMinnesotaNorth DakotaSouth DakotaWisconsin

Stores named: Walmart

Questions about this recall

Is Triple Berry Parfait recalled?

Yes. Russ Davis Wholesale recalled Triple Berry Parfait on 29 Jul 2022. The recall is Class II and its status is Terminated. Recall number F-1757-2022.

Why was it recalled?

Various vegetable and fruit products are recalled due to inadequate sanitizer in wash water.

Which lots are affected?

1. Lot Code: X5950748, X5950748, X5955610, X5950748, X5955610, X5957211, X5955610, X5955610, X5957211, X5960185, X5955610, X5960185, X5961784, X5960185, X5961784, X5965071, X5961784, X5965071, X5967083, X5965071, X5967083, X5970251, X5967083, X5970251, X5973394, X5970251, X5973394, X5976408, X5978626, X5973394, X5976408, X5978626, X5976408, X5978626, X5981915, X5978626, X5981915, X5984747, X5981915, X5984747, X5987204, X5984747, X5987204, X5990635, X5987204, X5990635, X5993277, X5990635, X5993277, X5996223, X5993277, X5996223, X5998844, X5996223, X5998844. Use by Dates: 7/13-8/3/2022 2. Lot Code: X5953078, X5956997, X5959085, X5962068, X5967308, X5964566, X5967308, X5969823, X5973066, X5975958, X5978859, X5981505, X5984210, X5986763, X5990384, X5992845, X5995680, X5998398, X6001019. Use by Dates: 7/13-8/3/2022

Where was it sold?

IA, MI, MN, ND, SD, WI

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 II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 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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