Strawberry & Pineapple. Packaged in the following brands and sizes: 1. Item 80640. Net Wt. 14 oz. Crazy Fresh 2.
Summary
The FDA issued a Class II for Strawberry & Pineapple. Packaged in the following brands and sizes: 1. Item by Russ Davis Wholesale, LLC. Reason: Various vegetable and fruit products are recalled due to inadequate sanitizer in wash water..
Details
Source
Food Recall
External ID
F-1755-2022
Action Date
2022-09-28
Status
Terminated
Category
food
Product Description
Strawberry & Pineapple. Packaged in the following brands and sizes: 1. Item 80640. Net Wt. 14 oz. Crazy Fresh 2. Item 80868. Net Wt 20 oz. Crazy Fresh, quick & easy, and grocery store branded. 3. Item 89274. Hawaiian Crush Net Wt. 16 oz. Kowalski's Markets
Lot/Code Info: 1. Lot Code: X5981977, X5984646, X5989439, X5987266, X5993572, X5996294, X5998910. Use by Dates: 7/26-8/2/2022 2. Lot Code: X5981811, X5984484, X5989200, X5990978, X5993387, X5996075, X5998691. Use by Dates: 7/26-8/2/2022 3. Lot Code: X5986874, X5993027, X5998345. Use by Dates: 7/27-8/1/2022
Quantity Affected: 87,915 units total
Reason for Recall
Various vegetable and fruit products are recalled due to inadequate sanitizer in wash water.
Distribution
IA, MI, MN, ND, SD, WI
Type: Voluntary: Firm initiated
Recall Initiated: 2022-07-29
Company
Inver Grove Heights, MN
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 63 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Russ Davis Wholesale, LLC has 37 FDA actions in our database, including 37 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Russ Davis Wholesale, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Russ Davis Wholesale, LLC have FDA actions?
Russ Davis Wholesale, LLC has 37 FDA actions in our database, including 37 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1755-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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