CLASS I Food recall · Reported 4 May 2016 · FDA Enforcement Report

Taste of Inspirations Edamame Rangoon ., frozen recalled

Progressive Gourmet is recalling Taste of Inspirations Edamame Rangoon ., frozen, distributed in Maine, New York. The recall was initiated on 7 Apr 2016 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesUse By 01/11/2017
Quantity recalled70 cases(12/case)

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-1128-2016
FDA event ID
73798
Recalling firm
Progressive Gourmet, Wilmington, MA
Brand
Taste
Classification
Class I
Status
Terminated
Recall initiated
7 Apr 2016
FDA classified
22 Apr 2016
Reported
4 May 2016
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Undeclared Allergens
Product category
Beans & Lentils

Timeline

7 Apr 2016Recall initiated by company
22 Apr 2016Classified by FDA+15 days
4 May 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

Product contains undeclared allergen-crabmeat

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

Taste of Inspirations Edamame Rangoon 9 oz . carton, frozen UPC: 072543998453

Where it was distributed

NY , ME

MaineNew York

Questions about this recall

Why was it recalled?

Product contains undeclared allergen-crabmeat

Which lots are affected?

Use By 01/11/2017

Where was it sold?

NY , ME

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 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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