FDA recall record

Myanmar Wholesale Trading Thanlwin Fried Bean Snack, Net Weight 227 g 8 oz recall — FDA F-0038-2018

Thanlwin Fried Bean Snack is being recalled due to undeclared peanuts.

Class Iclassification
F-0038-2018official record ID
Nov 1, 2017report date

Recall record at a glance

Official recordF-0038-2018
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmMyanmar Wholesale Trading
Report dateNov 1, 2017
Recall initiation dateOct 18, 2017
Quantity92 Cases
LocationMaplewood, MN, United States

Official product description

Thanlwin Fried Bean Snack, Net Weight 227 g 8 oz.. UPC 84682-00095 Product of Myanmar.

Why the product was recalled

Thanlwin Fried Bean Snack is being recalled due to undeclared peanuts.

Distribution information

IA, IL, IN, and MN

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: 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.