FDA recall record

O'Pelle Enterprises Opelle Bakery Rainbow Bagel recall — FDA F-1332-2017

The Rainbow Bagel flavor label lacks declaration of Yellow 5, Yellow 6, Blue 1, Red 40 and Red 3 on its label.

Class IIclassification
F-1332-2017official record ID
Jan 25, 2017report date

Recall record at a glance

Official recordF-1332-2017
CategoryFood Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmO'Pelle Enterprises, Inc.
Report dateJan 25, 2017
Recall initiation dateDec 9, 2016
Quantity53 cases still within shelf-life at initiation of recall
LocationPompano Beach, FL, United States

Official product description

Opelle Bakery Rainbow Bagel (B-110), case of 96 (4 oz.), Frozen Raw.

Why the product was recalled

The Rainbow Bagel flavor label lacks declaration of Yellow 5, Yellow 6, Blue 1, Red 40 and Red 3 on its label.

Distribution information

Distributed only within Florida.

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: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

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.