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Driscoll's Inc. 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

United States

TerminatedClass III

Company
Driscoll's Inc.
Product
Driscoll's Conventional Strawberries (Fresh) packed in 8x16o…
Recall date
January 21, 2022
Terminated
February 16, 2022
Source
FDA

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

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
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. Not published in this source record 8,222 crates 14-9725-0117, 14-9725-0118, 14-9725-0119. 14-101911- 0117, 14-101911- 0118, 14-101911- 0119.

Distribution

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

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0737-2022
Event ID
89578
Status
Terminated
Classification
Class III
Company
Driscoll's Inc.
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.
Quantity
8,222 crates
Reason
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
Recall initiation date
January 21, 2022
Report date
February 23, 2022
Classification date
Not published in this source record
Termination date
February 16, 2022
Distribution pattern
Distributed to retail DCs in U.S. (CA, OK, MN, MO, MD); product may have been further distributed to CAN (ON)
UPC, lot, and code information
14-9725-0117, 14-9725-0118, 14-9725-0119. 14-101911- 0117, 14-101911- 0118, 14-101911- 0119.
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Driscoll's Inc.

Other recalls from Driscoll's Inc.

FDA Recall United States Terminated Historical recordClass III

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Product
Driscoll's Blackberries (Fresh) 12x6 oz, 12x12 oz, 12x10 oz…
Published
May 25, 2022
Distribution
Product shipped to 13 DC's located in CA…

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FDA Recall United States Terminated Historical recordClass II

Driscoll's Inc.

Product
Driscolls's Fresh Blueberries 6 oz. and 1 pt. clamshell con…
Published
October 20, 2021
Distribution
Multiple states

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FDA Recall United States Terminated Historical recordClass II

Driscoll's Inc.

Product
Driscoll's Only the Finest Berries - Blueberries/ Bluets 6…
Published
October 6, 2021
Distribution
USA, Canada, Middle East

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Distribution map

A map highlighting the states named in the source's distribution description.

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map
State Distributed
California 1
Oklahoma 1
Minnesota 1
Missouri 1
Maryland 1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class III mean?

A situation in which use of or exposure to a product is not likely to cause adverse health consequences.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.