Check the Batch
Class IIITerminated in FDA datasetRecall initiated Dec 4, 2017

Publix brand, item # 41596, Southern Style Diced Hash Brown Potatoes, Net wt. 32 oz. Retail's

Recalling firm: McCain Foods USA

Why it was recalled

Publix brand Southern Style Diced Hash Brown Potatoes, net wt. 32 oz. package, is recalled because the firm received consumer complaints that foreign material was found in product.

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 28, 2018.

Check your package

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

ProductPublix brand, item # 41596, Southern Style Diced Hash Brown Potatoes, Net wt. 32 oz. Retail's UPC # 0 41415 00549 5. The label is read in parts: "***Publix Southern Style DICED HASH BROWN POTATOES***DISTRIBUTED BY PUBLIX SUPERMARKETS, INC. LAKELAND, FL 33802***".
Package size32 oz
UPC041415005495

FDA code information

B170322 is shown on package. batch # 1002167476

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

Full FDA record and distribution details

Original product description

Publix brand, item # 41596, Southern Style Diced Hash Brown Potatoes, Net wt. 32 oz. Retail's UPC # 0 41415 00549 5. The label is read in parts: "***Publix Southern Style DICED HASH BROWN POTATOES***DISTRIBUTED BY PUBLIX SUPERMARKETS, INC. LAKELAND, FL 33802***".

Extracted codes and context

TypeCode / valueContext
UPC041415005495 41596, Southern Style Diced Hash Brown Potatoes, Net wt. 32 oz. Retail's UPC # 0 41415 00549 5. The label is read in parts: "***Publix Southern Style DICED HASH BROWN POTATOES***DISTRIBUTED BY PUBLIX SUPERMARKET
batch1002167476B170322 is shown on package. batch # 1002167476

Original FDA recall reason

Publix brand Southern Style Diced Hash Brown Potatoes, net wt. 32 oz. package, is recalled because the firm received consumer complaints that foreign material was found in product.

Recall details

Recall number
F-0534-2018
Event ID
78689
FDA status
Terminated
Initiated
Dec 4, 2017
Reported
Jan 17, 2018
Classified
Jan 8, 2018
Terminated
Feb 28, 2018
Quantity
1463 cases
Location
Lisle, IL, United States
Initiation type
Voluntary: Firm initiated
Notification
Telephone

Where it was distributed

distributed in FL

FDA source record · F-0534-2018

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

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