CLASS III Food recall · Reported 13 Apr 2016 · FDA Enforcement Report

Novo Bnei Darom Green Olives recalled by International Trading &

International Trading & Import I is recalling Novo Bnei Darom Green Olives. The recall was initiated on 4 Mar 2016 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codesKD71 4126
Quantity recalled48 cases

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-1042-2016
FDA event ID
73476
Recalling firm
International Trading & Import I, Culver City, CA
Classification
Class III
Status
Terminated
Recall initiated
4 Mar 2016
FDA classified
7 Apr 2016
Reported
13 Apr 2016
Type
Voluntary: Firm initiated
Customers notified by
Letter
Product category
Fish

Timeline

4 Mar 2016Recall initiated by company
7 Apr 2016Classified by FDA+34 days
13 Apr 2016Published in enforcement report+6 days

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

Reason for recall

International Trading & Import Inc. dba Nuts & More is recalling Novo Bnei Darom Green Olives because it contains an unapproved pesticide (Chlorpyrifos)

Products marketed as supplements sometimes contain undeclared prescription drug ingredients such as sildenafil or sibutramine. These can interact dangerously with other medicines.

Product as listed by the FDA

Novo Bnei Darom Green Olives in Jar, 48 cases, 6 jars, 1.04kg, UPC Code 7290002016175

Where it was distributed

US

Questions about this recall

Why was it recalled?

International Trading & Import Inc. dba Nuts & More is recalling Novo Bnei Darom Green Olives because it contains an unapproved pesticide (Chlorpyrifos)

Which lots are affected?

KD71 4126

Where was it sold?

US

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 III mean?

Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.

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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