Check the Batch
Class IITerminated in FDA datasetRecall initiated Apr 29, 2016

Doctor Kracker Pumpkin Seed Cheddar Crispbreads Net Wt. 7 oz. (200g) in cardboard container.

Recalling firm: Kracker Enterprises, LLC

Why it was recalled

Undeclared milk in the ingredient statement although the product name contains Cheddar.

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 13, 2017.

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Compare the exact product and package details with the label you have.

ProductDoctor Kracker Pumpkin Seed Cheddar Crispbreads Net Wt. 7 oz. (200g) in cardboard container.
Package size7 oz

FDA code information

UPC: 95538 00002, Lot Number: 170216316070, 170219216077, 170223616091, 170229216105, 170232816117

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

Doctor Kracker Pumpkin Seed Cheddar Crispbreads Net Wt. 7 oz. (200g) in cardboard container.

Extracted codes and context

TypeCode / valueContext
lot170216316070UPC: 95538 00002, Lot Number: 170216316070, 170219216077, 170223616091, 170229216105, 170232816117
lot170219216077UPC: 95538 00002, Lot Number: 170216316070, 170219216077, 170223616091, 170229216105, 170232816117
lot170223616091UPC: 95538 00002, Lot Number: 170216316070, 170219216077, 170223616091, 170229216105, 170232816117
lot170229216105UPC: 95538 00002, Lot Number: 170216316070, 170219216077, 170223616091, 170229216105, 170232816117
lot1702328161175538 00002, Lot Number: 170216316070, 170219216077, 170223616091, 170229216105, 170232816117

Original FDA recall reason

Undeclared milk in the ingredient statement although the product name contains Cheddar.

Recall details

Recall number
F-0043-2017
Event ID
74001
FDA status
Terminated
Initiated
Apr 29, 2016
Reported
Oct 19, 2016
Classified
Oct 7, 2016
Terminated
Mar 13, 2017
Quantity
7125 cases
Location
Plano, TX, 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

CA, IA, IL, MD, MO, NY, RI, TX, WA, WI

FDA source record · F-0043-2017

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

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