CLASS II Food recall · Reported 5 Sep 2018 · FDA Enforcement Report

Dill was recalled by Howard Calcagno Farms

Howard Calcagno Farms is recalling Dill was, distributed in Oregon. The recall was initiated on 13 Aug 2018 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesNone
Quantity recalled6 ct

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-1927-2018
FDA event ID
80816
Recalling firm
Howard Calcagno Farms, Aurora, OR
Brand
Dill
Classification
Class II
Status
Terminated
Recall initiated
13 Aug 2018
FDA classified
28 Aug 2018
Reported
5 Sep 2018
Type
Voluntary: Firm initiated
Customers notified by
Telephone
Reason category
Other Reasons
Product category
Fresh Herbs

Timeline

13 Aug 2018Recall initiated by company
28 Aug 2018Classified by FDA+15 days
5 Sep 2018Published in enforcement report+8 days

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

Reason for recall

Dill is recalled due to a potential for contamination with Cyclospora cayetanensis.

Product as listed by the FDA

Dill was shipped in card board boxes that are labeled with the firm name "Howard Calcagno, Aurora, OR 97002".

Where it was distributed

distributed in Oregon

Oregon

Questions about this recall

Is Dill was recalled?

Yes. Howard Calcagno Farms recalled Dill was on 13 Aug 2018. The recall is Class II and its status is Terminated. Recall number F-1927-2018.

Why was it recalled?

Dill is recalled due to a potential for contamination with Cyclospora cayetanensis.

Which lots are affected?

None

Where was it sold?

distributed in Oregon

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 II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 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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