Class ITerminated in FDA datasetRecall initiated Jan 14, 2016

Uncle Buck's Fish Batter Mix Original, packaged in 22 oz. (623 g) plastic bottles, bottle lot…

Recalling firm: BlendTech Inc

Why it was recalled

Product contains an undeclared milk ingredient.

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: Feb 8, 2017.

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ProductUncle Buck's Fish Batter Mix Original, packaged in 22 oz. (623 g) plastic bottles, bottle lot #09241505, UPC 09229725284 and packed 12 bottles/case. Bottles were shipped in cases under lot #09241506 and lot #09241507. Produced and Packaged in the USA for Bass Pro Shops By Monogram Food Solutions, LLC, Memphis, TN 38117.
Package size22 oz

FDA code information

bottle: lot #09241505 case: lot #09241506 and #09241507

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Full FDA record and distribution details

Original product description

Uncle Buck's Fish Batter Mix Original, packaged in 22 oz. (623 g) plastic bottles, bottle lot #09241505, UPC 09229725284 and packed 12 bottles/case. Bottles were shipped in cases under lot #09241506 and lot #09241507. Produced and Packaged in the USA for Bass Pro Shops By Monogram Food Solutions, LLC, Memphis, TN 38117.

Extracted codes and context

TypeCode / valueContext
lot09241505bottle: lot #09241505 case: lot #09241506 and #09241507
lot09241505sh Batter Mix Original, packaged in 22 oz. (623 g) plastic bottles, bottle lot #09241505, UPC 09229725284 and packed 12 bottles/case. Bottles were shipped in cases under lot #09241506 and lot #09241507. Pr

Original FDA recall reason

Product contains an undeclared milk ingredient.

Recall details

Recall number
F-0600-2016
Event ID
73079
FDA status
Terminated
Initiated
Jan 14, 2016
Reported
Feb 24, 2016
Classified
Feb 17, 2016
Terminated
Feb 8, 2017
Quantity
3,360 bottles (280 cases)
Location
Wichita, KS, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

Recalling firm sent product to one distributor in Springfield, MO. Distributor further distributed product nationwide. There was no foreign, military, or government distribution.

FDA source record · F-0600-2016

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

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