CLASS I Food recall · Reported 26 Oct 2016 · FDA Enforcement Report

Birdy 1 Robusta Coffea Mix in a red sealed recalled by Food Gusto

Food Gusto is recalling Birdy 1 Robusta Coffea Mix in a red sealed, distributed in Connecticut, Massachusetts, New York. The recall was initiated on 10 May 2016 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot #D092121515
Quantity recalled30 cartons

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-0189-2017
FDA event ID
74159
Recalling firm
Food Gusto, Paterson, NJ
Brand
Birdy
Classification
Class I
Status
Terminated
Recall initiated
10 May 2016
FDA classified
19 Oct 2016
Reported
26 Oct 2016
Type
Voluntary: Firm initiated
Customers notified by
Telephone
Reason category
Undeclared Milk
Product category
Other

Timeline

10 May 2016Recall initiated by company
19 Oct 2016Classified by FDA+162 days
26 Oct 2016Published in enforcement report+7 days

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

Reason for recall

Birdy 3 in 1 Coffee Mix (Robusta) may contain undeclared milk allergen and the nutritional labeling is unclear.

Product as listed by the FDA

Birdy 3 in 1 Robusta Coffea Mix, 445.5 g in a red sealed plastic bag, Product of Thailand, UPC 8850250007425

Where it was distributed

CT, MA and NY

ConnecticutMassachusettsNew York

Questions about this recall

Why was it recalled?

Birdy 3 in 1 Coffee Mix (Robusta) may contain undeclared milk allergen and the nutritional labeling is unclear.

Which lots are affected?

Lot #D092121515

Where was it sold?

CT, MA and NY

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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