RecallHawk
Class I Recall

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

Supherb Farms

Summary

The FDA issued a Class I for IQF Fresh Frozen Dill shipped in 35 lb. cases in bulk. Supherb Farms Turlock, C by Supherb Farms. Reason: RTE Frozen Dill is being recalled after a customer tested product and Listeria Monocytogenes was found to be present.

Details

Source

Food Recall

External ID

F-1585-2022

Action Date

2022-09-07

Status

Terminated

Category

food

Product Description

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

Lot/Code Info: 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

Quantity Affected: 25,009 pounds

Reason for Recall

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

Distribution

Nationwide and Canada

Type: Voluntary: Firm initiated

Recall Initiated: 2022-08-11

Company

Supherb Farms

Turlock, CA

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

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

Supherb Farms has 3 FDA actions in our database, including 3 recalls.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

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 (Supherb Farms) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Supherb Farms have FDA actions?

Supherb Farms has 3 FDA actions in our database, including 3 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1585-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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