Class ITerminated in FDA datasetRecall initiated Jun 22, 2013

Sani Fresh Distribution brand MINI KAISER 10, Net Weight 13 OZ, Product of Canada

Recalling firm: Sani Fresh Distribution

Why it was recalled

Canadian firm recalled Mini Kaiser 10 due to undeclared soy in the product. The product was also found to contain undeclared wheat, sulfites, soybean oil and gluten (barley and/or…

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Mar 30, 2017.

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ProductSani Fresh Distribution brand MINI KAISER 10, Net Weight 13 OZ, Product of Canada, UPC 0 56931 51125 2 --- DISTRIBUTED BY SANI BAKERY INC. 28-24 STEINWAY ST., SUITE 108, ASTORIA NY 11103 --- The mini kaisers are packed in clear plastic sealed bags (contain 10 rolls per bag) which are placed in unmarked brown boxes/cartons. The product has a short shelf life.
Package size13 OZ
UPC056931511252

FDA code information

UPC 0 56931 51125 2 and no other coding

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Full FDA record and distribution details

Original product description

Sani Fresh Distribution brand MINI KAISER 10, Net Weight 13 OZ, Product of Canada, UPC 0 56931 51125 2 --- DISTRIBUTED BY SANI BAKERY INC. 28-24 STEINWAY ST., SUITE 108, ASTORIA NY 11103 --- The mini kaisers are packed in clear plastic sealed bags (contain 10 rolls per bag) which are placed in unmarked brown boxes/cartons. The product has a short shelf life.

Extracted codes and context

TypeCode / valueContext
UPC056931511252UPC 0 56931 51125 2 and no other coding
UPC056931511252esh Distribution brand MINI KAISER 10, Net Weight 13 OZ, Product of Canada, UPC 0 56931 51125 2 --- DISTRIBUTED BY SANI BAKERY INC. 28-24 STEINWAY ST., SUITE 108, ASTORIA NY 11103 --- The mini kaisers are packed in

Original FDA recall reason

Canadian firm recalled Mini Kaiser 10 due to undeclared soy in the product. The product was also found to contain undeclared wheat, sulfites, soybean oil and gluten (barley and/or rye) all from the Doughmaster 200 raw material.

Recall details

Recall number
F-1724-2013
Event ID
65581
FDA status
Terminated
Initiated
Jun 22, 2013
Reported
Jul 24, 2013
Classified
Jul 18, 2013
Terminated
Mar 30, 2017
Quantity
93 cartons
Location
Long Island City, NY, United States
Initiation type
Voluntary: Firm initiated
Notification
Visit

Where it was distributed

Borough of Queens, NY

FDA source record · F-1724-2013

Data updated September 16, 2026. View official FDA data ↗

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