RecallHawk
Class III Recall

Driscoll's Conventional Strawberries (Fresh) packed in 8x16oz clamshell and 4X32oz clamshell; 8 clamshells per case, 4

Driscoll's Inc.

Summary

The FDA issued a Class III for Driscoll's Conventional Strawberries (Fresh) packed in 8x16oz clamshell and 4X32 by Driscoll's Inc.. Reason: Driscoll s identified specific lots of strawberries exceeding the United States Maximum Residual Limit (MRL) for the pesticide Etoxazole. Analytical .

Details

Source

Food Recall

External ID

F-0737-2022

Action Date

2022-02-23

Status

Terminated

Category

food

Product Description

Driscoll's Conventional Strawberries (Fresh) packed in 8x16oz clamshell and 4X32oz clamshell; 8 clamshells per case, 4 clamshells per case, respectively. Harvest date: Jan-17-2022, Jan-18-2022, Jan-19-2022.

Lot/Code Info: 14-9725-0117, 14-9725-0118, 14-9725-0119. 14-101911- 0117, 14-101911- 0118, 14-101911- 0119.

Quantity Affected: 8,222 crates

Reason for Recall

Driscoll s identified specific lots of strawberries exceeding the United States Maximum Residual Limit (MRL) for the pesticide Etoxazole. Analytical results included residue level between 1.20 to 1.28 ppm

Distribution

Distributed to retail DCs in U.S. (CA, OK, MN, MO, MD); product may have been further distributed to CAN (ON)

Type: Voluntary: Firm initiated

Recall Initiated: 2022-01-21

Company

Driscoll's Inc.

Watsonville, CA

Context & Analysis

This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.

This was one of 111 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Driscoll's Inc. has 4 FDA actions in our database, including 4 recalls.

Frequently Asked Questions

What is a Class III recall?

A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.

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 (Driscoll's Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Driscoll's Inc. have FDA actions?

Driscoll's Inc. has 4 FDA actions in our database, including 4 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0737-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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