CLASS I Food recall · Reported 7 Sep 2022 · FDA Enforcement Report

IQF Fresh Frozen Dill recalled by Supherb Farms

Supherb Farms is recalling IQF Fresh Frozen Dill, distributed nationwide in the US. The recall was initiated on 11 Aug 2022 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot 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
Quantity recalled25,009 pounds

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-1585-2022
FDA event ID
90741
Recalling firm
Supherb Farms, Turlock, CA
Classification
Class I
Status
Terminated
Recall initiated
11 Aug 2022
FDA classified
26 Aug 2022
Reported
7 Sep 2022
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Listeria
Product category
Fresh Herbs

Timeline

11 Aug 2022Recall initiated by company
26 Aug 2022Classified by FDA+15 days
7 Sep 2022Published in enforcement report+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

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

Listeria monocytogenes can grow at refrigerator temperatures. Infection is most dangerous for pregnant women, newborns, older adults and people with weakened immune systems. Symptoms can appear up to 70 days after eating contaminated food.

Product as listed by the FDA

IQF Fresh Frozen Dill shipped in 35 lb. cases in bulk. Supherb Farms Turlock, CA Perishable, Keep Frozen

Where it was distributed

Nationwide and Canada

Nationwide

Questions about this recall

Why was it recalled?

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

Which lots are affected?

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

Where was it sold?

Nationwide and Canada

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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