FDA recall record

Food Gusto Birdy 3 in 1 Robusta Coffea Mix, 445.5 g in a red sealed recall — FDA F-0189-2017

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

Class Iclassification
F-0189-2017official record ID
Oct 26, 2016report date

Recall record at a glance

Official recordF-0189-2017
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmFood Gusto, Inc.
Report dateOct 26, 2016
Recall initiation dateMay 10, 2016
Quantity30 cartons
LocationPaterson, NJ, United States

Official product description

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

Why the product was recalled

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

Distribution information

CT, MA and NY

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Telephone.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.