CLASS I Food recall · Reported 24 Feb 2016 · FDA Enforcement Report

Uncle Buck's Fish Batter Mix Original recalled by BlendTech

BlendTech is recalling Uncle Buck's Fish Batter Mix Original, distributed nationwide in the US. The recall was initiated on 14 Jan 2016 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesbottle: lot #09241505 case: lot #09241506 and #09241507
Quantity recalled3,360 bottles (280 cases)

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0600-2016
FDA event ID
73079
Recalling firm
BlendTech, Wichita, KS
Classification
Class I
Status
Terminated
Recall initiated
14 Jan 2016
FDA classified
17 Feb 2016
Reported
24 Feb 2016
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Undeclared Milk
Product category
Fish

Timeline

14 Jan 2016Recall initiated by company
17 Feb 2016Classified by FDA+34 days
24 Feb 2016Published in enforcement report+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Product contains an undeclared milk ingredient.

Product as listed by the FDA

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.

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.

Nationwide Missouri

Questions about this recall

Why was it recalled?

Product contains an undeclared milk ingredient.

Which lots are affected?

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

Where was it sold?

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

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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