FDA Food Recalls

Recalls / Class II

Class IIF-1761-2022

Product

Cauliflower packaged in the following forms and brands: 1. Item 80836. Cauliflower Steak Net Wt. 12 oz. Keep Refrigerated. Crazy Fresh, quick & easy, and grocery store branded. 2. Item 82383 Cauliflower Florets Net Wt. 3 lbs. Keep Refrigerated. grocery store branded. 3. Item 82556 Cauliflower Florets Net Wt. 5 lbs. Keep Refrigerated. grocery store branded. 4. Item 89291 Cauliflower Steaks Net Wt. 20 oz. Keep Refrigerates. Kowalski's Markets.

Type
Food
Affected lot / code info
1. Lot Code: X5947964, X5948932, X5952780, X5955333, X5959270, X5961627, X5964613, X5966932, X5968556, X5972165, X5976015, X5977312, X5981576, X5984229, X5985219, X5989186, X5992956, X5993995, X5998451, X5999575. Use by Dates: 7/13-8/4/2022 2. Lot Code: X5947971, X5950593, X5953220, X5955578, X5959275, X5962041, X5964622, X5967348, X5969975, X5972223, X5972223, X5976022, X5978878, X5981587, X5984237, X5986824, X5989244, X5992963, X5995755, X5998459, X6001097. Use by Dates: 7/13-8/4/2022 3. Lot Code: X5947979, X5953228, X5964630, X5967356, X5969983, X5972433, X5976029, X5981595, X5984245, X5992970, X5995762, X6001239. Use by Dates: 7/13-8/4/2022 4. Lot Code: X5947936, X5950643, X5953055, X5956899, X5959141, X5962021, X5964689, X5967389, X5969891, X5973256, X5976083, X5978927, X5981641, X5984288, X5986886, X5990554, X5993039, X5995810, X5998357, X6001151. Use by Dates:7/13-8/4/2022
Quantity
87,915 units total

Why it was recalled

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

Recalling firm

Firm
Russ Davis Wholesale, LLC
Notification channel
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Type
Voluntary: Firm initiated
Address
6085 Claude Way, N/A, Inver Grove Heights, Minnesota 55076-4432

Distribution

Distribution pattern
IA, MI, MN, ND, SD, WI

Timeline

Recall initiated
2022-07-29
FDA classified
2022-09-22
Posted by FDA
2022-09-28
Terminated
2022-09-23
Status
Terminated

Source: openFDA Food Enforcement endpoint. Recall record F-1761-2022. The FDA issues recall classifications as health-hazard assessments, not legal findings.