CLASS II Food recall · Reported 12 Aug 2015 · FDA Enforcement Report

Pistachio-Pistache popsicle, La Jalpita recalled by Paleteria La Jalpita

Paleteria La Jalpita is recalling Pistachio-Pistache popsicle, La Jalpita, distributed in Oregon, Washington. The recall was initiated on 29 May 2015 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesNone
Quantity recalled740 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-2925-2015
FDA event ID
71379
Recalling firm
Paleteria La Jalpita, Pasco, WA
Classification
Class II
Status
Terminated
Recall initiated
29 May 2015
FDA classified
3 Aug 2015
Reported
12 Aug 2015
Type
Voluntary: Firm initiated
Customers notified by
Press Release
Reason category
Undeclared Allergens

Timeline

29 May 2015Recall initiated by company
3 Aug 2015Classified by FDA+66 days
12 Aug 2015Published in enforcement report+9 days

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

Reason for recall

Pistachio-Pistache popsicle is recalled due to undeclared Yellow no. 5

Food allergen labelling is required by US law for the nine major allergens. A product recalled for an undeclared allergen is only a risk to people with that allergy; everyone else can consume it safely.

Product as listed by the FDA

Pistachio-Pistache popsicle, La Jalpita brand, 3 Fl oz, UPC 651821269758.

Where it was distributed

distributed in Oregon and Washington

OregonWashington

Questions about this recall

Why was it recalled?

Pistachio-Pistache popsicle is recalled due to undeclared Yellow no. 5

Which lots are affected?

None

Where was it sold?

distributed in Oregon and Washington

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.

Other products in this recall event

11 other products · FDA event 71379

This product is part of a recall event; the main page for the event is Vanilla bolis (tube), La Jalpita brand, No recalled.

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