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
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 2016 | Recall initiated by company | |
| 19 Oct 2016 | Classified by FDA | +162 days |
| 26 Oct 2016 | Published 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
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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