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Supherb Farms Recall: RTE Frozen Dill is being recalled after a customer tested product and Listeria Monocytogenes was found to be present

United States

TerminatedClass I

Company
Supherb Farms
Product
IQF Fresh Frozen Dill shipped in 35 lb. cases in bulk. Suph…
Recall date
August 11, 2022
Terminated
October 4, 2022
Source
FDA

Reason for recall

RTE Frozen Dill is being recalled after a customer tested product and Listeria Monocytogenes was found to be present

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
IQF Fresh Frozen Dill shipped in 35 lb. cases in bulk. Supherb Farms Turlock, CA Perishable, Keep Frozen Not published in this source record 25,009 pounds Lot code interpretation: 035720-11.19.21 Unique ID 6 digit code - Production date Product code:11210 Lot: 035720-11.19.21 Product code:11210 Lot: 035727-11.19.21 Product code:11210 Lot: 035731-11.19.21 Product code:10120 Lot: 036367-03.23.22 Product code:16598 Lot: 035932-12.17.21 Product code:17058 Lot: 035930-12.17.21 NET WT: 35 LBS Code 11210, 10120, 16598

Distribution

  • Nationwide and Canada

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-1585-2022
Event ID
90741
Status
Terminated
Classification
Class I
Company
Supherb Farms
Product description
IQF Fresh Frozen Dill shipped in 35 lb. cases in bulk. Supherb Farms Turlock, CA Perishable, Keep Frozen
Quantity
25,009 pounds
Reason
RTE Frozen Dill is being recalled after a customer tested product and Listeria Monocytogenes was found to be present
Recall initiation date
August 11, 2022
Report date
September 7, 2022
Classification date
Not published in this source record
Termination date
October 4, 2022
Distribution pattern
Nationwide and Canada
UPC, lot, and code information
Lot code interpretation: 035720-11.19.21 Unique ID 6 digit code - Production date Product code:11210 Lot: 035720-11.19.21 Product code:11210 Lot: 035727-11.19.21 Product code:11210 Lot: 035731-11.19.21 Product code:10120 Lot: 036367-03.23.22 Product code:16598 Lot: 035932-12.17.21 Product code:17058 Lot: 035930-12.17.21 NET WT: 35 LBS Code 11210, 10120, 16598
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
E-Mail
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Supherb Farms

Other recalls from Supherb Farms

FDA Recall United States Completed Historical recordClass II

Supherb Farms

Product
Label: FROZEN CHOPPED CILANTRO; PACK SIZE: 4 - 8 oz; NET WT:…
Published
April 30, 2025
Distribution
United States: CA, MA, MI, NY, OH, OR, T…

View recall →

FDA Recall United States Completed Historical recordClass II

Supherb Farms

Product
Label: IQF CILANTRO LARGE; NET WT: 30LB; PERISHABLE KEEP FRO…
Published
April 30, 2025
Distribution
United States: CA, MA, MI, NY, OH, OR, T…

View recall →

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 I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

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.