RecallHawk
Class III Recall

Driscoll's Blackberries (Fresh) 12x6 oz, 12x12 oz, 12x10 oz, 2x8x18 oz Clamshell Distributed by Strawberry Associated,

Driscoll's Inc.

Summary

The FDA issued a Class III for Driscoll's Blackberries (Fresh) 12x6 oz, 12x12 oz, 12x10 oz, 2x8x18 oz Clamshel by Driscoll's Inc.. Reason: California Department of Pesticide Regulation detected the presence of Formetante HCI. This pesticide has a non-tolerance for blackberries..

Details

Source

Food Recall

External ID

F-1067-2022

Action Date

2022-05-25

Status

Terminated

Category

food

Product Description

Driscoll's Blackberries (Fresh) 12x6 oz, 12x12 oz, 12x10 oz, 2x8x18 oz Clamshell Distributed by Strawberry Associated, Inc. Watsonville, CA Product of Mexico

Lot/Code Info: Lot # 1100-9133-0403, 1100-9133-0404, 1100-9133-0405, 1100-9133-0406, 1100-9133-0407, 1100-9133-0408, 1100-9133-0409, 1100-9133-0410, 1100-9133-0411

Quantity Affected: 1,293 crates

Reason for Recall

California Department of Pesticide Regulation detected the presence of Formetante HCI. This pesticide has a non-tolerance for blackberries.

Distribution

Product shipped to 13 DC's located in CA, TX, OR, IL, MD, FL, NC, WI

Type: Voluntary: Firm initiated

Recall Initiated: 2022-04-15

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 25 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-1067-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

Want to know the moment something like this happens?

Get alerts for food

Related Actions