CLASS III Food recall · Reported 30 Mar 2016 · FDA Enforcement Report

HEB Creamy Creations Caramel Pecan Turtle Ice Cream Half Gallon/Cont recalled

HEB Retail Support Center is recalling HEB Creamy Creations Caramel Pecan Turtle Ice Cream Half Gallon/Cont, distributed in Texas. The recall was initiated on 4 Feb 2016 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codesSELL BY: 20 APR(ABR)16, 10 MAY(MAY)16, 07 JUN(JUN)16, 18 JUL(JUL)16
Quantity recalled37,432 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-0775-2016
FDA event ID
73236
Recalling firm
HEB Retail Support Center, San Antonio, TX
Classification
Class III
Status
Terminated
Recall initiated
4 Feb 2016
FDA classified
18 Mar 2016
Reported
30 Mar 2016
Type
Voluntary: Firm initiated
Customers notified by
Press Release
Reason category
Foreign Material

Timeline

4 Feb 2016Recall initiated by company
18 Mar 2016Classified by FDA+43 days
30 Mar 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

Wood pieces in the product.

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

HEB Creamy Creations Caramel Pecan Turtle Ice Cream Half Gallon/Cont. Net. 1.89 L packaged in cardboard container

Where it was distributed

Texas and Mexico.

Texas

Stores named: H-E-B

Questions about this recall

Why was it recalled?

Wood pieces in the product.

Which lots are affected?

SELL BY: 20 APR(ABR)16, 10 MAY(MAY)16, 07 JUN(JUN)16, 18 JUL(JUL)16

Where was it sold?

Texas and Mexico.

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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