FDA recall record

Baroody Imports Chiclets Chewing Gum Fruit Flavors recall — FDA F-1943-2012

Baroody Imports Inc. is voluntarily recalling Chiclets Chewing Gum (Fruit Flavors) due to Misbranded/Unsafe Color Additives.

Class IIclassification
F-1943-2012official record ID
Aug 22, 2012report date

Recall record at a glance

Official recordF-1943-2012
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmBaroody Imports Inc.
Report dateAug 22, 2012
Recall initiation dateMar 29, 2012
Quantity600 pcs
LocationClifton, NJ, United States

Official product description

Chiclets Chewing Gum Fruit Flavors; Made in Lebanon; Manufactured by Cadbury Adams Middle East S.A.L.

Why the product was recalled

Baroody Imports Inc. is voluntarily recalling Chiclets Chewing Gum (Fruit Flavors) due to Misbranded/Unsafe Color Additives.

Distribution information

The firm receives the gum from their overseas supplier and it is stored in their Clifton, NJ warehouse until the gum is shipped to 40 customers throughout the USA (OH, PA, NJ, NY, VA, and MA)

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA 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.

Related recall records

Other records from the same recalling company are shown first when available.