FDA recall record

Russ Davis Wholesale Strawberry, Blueberry, and Blackberry packaged in the recall — FDA F-1754-2022

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

Class IIclassification
F-1754-2022official record ID
Sep 28, 2022report date

Recall record at a glance

Official recordF-1754-2022
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmRuss Davis Wholesale, LLC
Report dateSep 28, 2022
Recall initiation dateJul 29, 2022
Quantity87,915 units total
LocationInver Grove Heights, MN, United States

Official product description

Strawberry, Blueberry, and Blackberry packaged in the following brands and sizes: 1. Item 80610. Triple Berry Blend Net Wt. 14 oz. Crazy Fresh 2. Item 80867. Triple Berry Blend Net Wt 20 oz. Crazy Fresh, quick & easy, and grocery store branded. 3. Item 89272. Berry Bliss Net Wt. 16 oz. Kowalski's Markets

Why the product was recalled

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

Distribution information

IA, MI, MN, ND, SD, WI

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

Related recall records

Other records from the same recalling company are shown first when available.