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Class ITerminated in FDA datasetRecall initiated Jun 25, 2026

Fresh to You Burger Chicken Fillet Deluxe with Bacon, SKU 10303, Net wt. 5.9oz. Product is…

Recalling firm: Fresh & Ready Foods LLC

Why it was recalled

Raw breaded chicken patties were inadvertently used in the ready to eat Burger Chicken Deluxe With Bacon sandwich. Raw breaded chicken patties pose a risk of foodborne illness due…

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: Aug 5, 2026.

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

ProductFresh to You Burger Chicken Fillet Deluxe with Bacon, SKU 10303, Net wt. 5.9oz. Product is refrigerated. UPC 1 00000 01030 3. Manufactured by LPK1 Renton, WA. Product was not sold at retail stores and sold only to employees at certain business' breakroom.
Package size5.9oz
UPC100000010303

FDA code information

Best By July 3, 2026, Lot 26171 Lot 26171 represents June 20, 2026.

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Full FDA record and distribution details

Original product description

Fresh to You Burger Chicken Fillet Deluxe with Bacon, SKU 10303, Net wt. 5.9oz. Product is refrigerated. UPC 1 00000 01030 3. Manufactured by LPK1 Renton, WA. Product was not sold at retail stores and sold only to employees at certain business' breakroom.

Extracted codes and context

TypeCode / valueContext
UPC100000010303llet Deluxe with Bacon, SKU 10303, Net wt. 5.9oz. Product is refrigerated. UPC 1 00000 01030 3. Manufactured by LPK1 Renton, WA. Product was not sold at retail stores and sold only to employees at certain business
best byJuly 3, 2026Best By July 3, 2026, Lot 26171 Lot 26171 represents June 20, 2026.

Original FDA recall reason

Raw breaded chicken patties were inadvertently used in the ready to eat Burger Chicken Deluxe With Bacon sandwich. Raw breaded chicken patties pose a risk of foodborne illness due to the potential presence of Salmonella.

Recall details

Recall number
H-1148-2026
Event ID
99335
FDA status
Terminated
Initiated
Jun 25, 2026
Reported
Jul 15, 2026
Classified
Jul 7, 2026
Terminated
Aug 5, 2026
Quantity
216 units
Location
Renton, WA, United States
Initiation type
Voluntary: Firm initiated
Notification
E-Mail

Where it was distributed

Distributed in OR and WA.

FDA source record · H-1148-2026

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

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