FDA recall record

Baily International Foods Wonton wrappers, 4" x 4" and 3.5" x 3.5", packaged in 30lb recall — FDA F-0621-2023

Peanut contamination (in sub ingredient)

Class IIIclassification
F-0621-2023official record ID
Mar 22, 2023report date

Recall record at a glance

Official recordF-0621-2023
CategoryFood Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmBaily International Foods
Report dateMar 22, 2023
Recall initiation dateFeb 22, 2023
Quantity24,516 corrugated (cardboard) boxes (19403 corrugated (cardboard) boxes of 4" x 4" and 5113 corrugated (cardboard) boxes of 3.5" x 3.5")
LocationFairmont City, IL, United States

Official product description

Wonton wrappers, 4" x 4" and 3.5" x 3.5", packaged in 30lb. corrugated (cardboard) boxes. Product is sold frozen.

Why the product was recalled

Peanut contamination (in sub ingredient)

Distribution information

Distributed to wholesalers in CO, FL, GA, IL, IA, KS, LA, MA, MI, MN, MS, MO, NE, NM, OH, TN, TX, UT, and WI; the wholesalers sell mainly to restaurants and institutions (not for consumer sales)

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

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.