CLASS II Food recall · Reported 14 Jul 2021 · FDA Enforcement Report

Hatch Verde Salsa Medium recalled by Heritage Family Specialty

Heritage Family Specialty Foods is recalling Hatch Verde Salsa Medium, distributed nationwide in the US. The recall was initiated on 14 Jun 2021 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot numbers: 11480042, 11550030, 11620032
Quantity recalled646 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-0786-2021
FDA event ID
88134
Recalling firm
Heritage Family Specialty Foods, Grand Prairie, TX
Classification
Class II
Status
Terminated
Recall initiated
14 Jun 2021
FDA classified
18 Jul 2021
Reported
14 Jul 2021
Type
Voluntary: Firm initiated
Customers notified by
Telephone
Reason category
Foreign Material
Product category
Dips & Spreads

Timeline

14 Jun 2021Recall initiated by company
14 Jul 2021Published in enforcement report+30 days
18 Jul 2021Classified by FDA+4 days

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

Reason for recall

Potential to contain a foreign material

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

Hatch Verde Salsa Medium Net Wt. 12 oz (340g) 6 jars per case packaged in clamshell container UPC Code: 810041591999

Where it was distributed

Nationwide

Nationwide

Questions about this recall

Why was it recalled?

Potential to contain a foreign material

Which lots are affected?

Lot numbers: 11480042, 11550030, 11620032

Where was it sold?

Nationwide

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

1 other product · FDA event 88134

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