CLASS II Food recall · Reported 27 Apr 2016 · FDA Enforcement Report

Hill Country Fare Chunk Light Tuna in pure vegetable oil recalled

HEB Retail Support Center is recalling Hill Country Fare Chunk Light Tuna in pure vegetable oil, distributed in Texas. The recall was initiated on 16 Mar 2016 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesUPC 041220653355 lot code 6O9FZ SCEES
Quantity recalled5,376 units

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-1083-2016
FDA event ID
73576
Recalling firm
HEB Retail Support Center, San Antonio, TX
Classification
Class II
Status
Terminated
Recall initiated
16 Mar 2016
FDA classified
15 Apr 2016
Reported
27 Apr 2016
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Foreign Material
Product category
Tuna

Timeline

16 Mar 2016Recall initiated by company
15 Apr 2016Classified by FDA+30 days
27 Apr 2016Published 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

The product may have been under processed.

Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.

Product as listed by the FDA

Hill Country Fare Chunk Light Tuna in pure vegetable oil NET WT. 5 OZ (142g) packaged in a metal can.

Where it was distributed

Texas

Texas

Stores named: H-E-B

Questions about this recall

Why was it recalled?

The product may have been under processed.

Which lots are affected?

UPC 041220653355 lot code 6O9FZ SCEES

Where was it sold?

Texas

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 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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