CLASS I Food recall · Reported 20 Jan 2016 · FDA Enforcement Report

Picosito Jalapenos recalled by Sweet Superior

Sweet Superior is recalling Picosito Jalapenos, distributed in Illinois, Texas. The recall was initiated on 11 Dec 2015 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLOT ORTI04
Quantity recalled1127 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-0469-2016
FDA event ID
72844
Recalling firm
Sweet Superior, Mcallen, TX
Classification
Class I
Status
Terminated
Recall initiated
11 Dec 2015
FDA classified
11 Jan 2016
Reported
20 Jan 2016
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Salmonella
Product category
Peppers

Timeline

11 Dec 2015Recall initiated by company
11 Jan 2016Classified by FDA+31 days
20 Jan 2016Published 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

Tested positive for Salmonella.

Salmonella causes fever, diarrhea and abdominal cramps, usually 12 to 72 hours after eating contaminated food. Most people recover without treatment, but severe cases can need hospital care.

Product as listed by the FDA

PICOSITO Jalapenos Distributed by: Sweet Superior Fruit LTD. CO. PRODUCE OF MEXICO

Where it was distributed

TX and IL

IllinoisTexas

Questions about this recall

Is Picosito Jalapenos recalled?

Yes. Sweet Superior recalled Picosito Jalapenos on 11 Dec 2015. The recall is Class I and its status is Terminated. Recall number F-0469-2016.

Why was it recalled?

Tested positive for Salmonella.

Which lots are affected?

LOT ORTI04

Where was it sold?

TX and IL

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 I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

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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