Check the Batch
Class ITerminated in FDA datasetRecall initiated May 1, 2015

Sub Way Apple Slices, 2.4 oz. Bags

Recalling firm: Sun Rich Fresh Foods Inc

Why it was recalled

Product has the potential to be contaminated with Listeria monocytogenes.

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: Jul 28, 2015.

Check your package

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

ProductSub Way Apple Slices, 2.4 oz. Bags
Package size2.4 oz

FDA code information

UPC Code:30825146031272; Best BY Date: 2015 MA 14; Lot Codes: 2510041; 2511041; 2512041; 2513041; 2514041; 2515041; 2517041; 2518041; 2519041; 2520041; 2521041; 2522041; 2524041; 2525041; 2526041

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

Full FDA record and distribution details

Original product description

Sub Way Apple Slices, 2.4 oz. Bags

Extracted codes and context

TypeCode / valueContext
lot2510041UPC Code:30825146031272; Best BY Date: 2015 MA 14; Lot Codes: 2510041; 2511041; 2512041; 2513041; 2514041; 2515041; 2517041; 2518041; 2519041; 2520041; 2521041; 2522041; 2524041; 2525041;
lot2511041UPC Code:30825146031272; Best BY Date: 2015 MA 14; Lot Codes: 2510041; 2511041; 2512041; 2513041; 2514041; 2515041; 2517041; 2518041; 2519041; 2520041; 2521041; 2522041; 2524041; 2525041; 2526041
lot2512041UPC Code:30825146031272; Best BY Date: 2015 MA 14; Lot Codes: 2510041; 2511041; 2512041; 2513041; 2514041; 2515041; 2517041; 2518041; 2519041; 2520041; 2521041; 2522041; 2524041; 2525041; 2526041
lot251304130825146031272; Best BY Date: 2015 MA 14; Lot Codes: 2510041; 2511041; 2512041; 2513041; 2514041; 2515041; 2517041; 2518041; 2519041; 2520041; 2521041; 2522041; 2524041; 2525041; 2526041
lot251404131272; Best BY Date: 2015 MA 14; Lot Codes: 2510041; 2511041; 2512041; 2513041; 2514041; 2515041; 2517041; 2518041; 2519041; 2520041; 2521041; 2522041; 2524041; 2525041; 2526041
lot2515041st BY Date: 2015 MA 14; Lot Codes: 2510041; 2511041; 2512041; 2513041; 2514041; 2515041; 2517041; 2518041; 2519041; 2520041; 2521041; 2522041; 2524041; 2525041; 2526041
lot2517041e: 2015 MA 14; Lot Codes: 2510041; 2511041; 2512041; 2513041; 2514041; 2515041; 2517041; 2518041; 2519041; 2520041; 2521041; 2522041; 2524041; 2525041; 2526041
lot2518041A 14; Lot Codes: 2510041; 2511041; 2512041; 2513041; 2514041; 2515041; 2517041; 2518041; 2519041; 2520041; 2521041; 2522041; 2524041; 2525041; 2526041
lot2519041 Codes: 2510041; 2511041; 2512041; 2513041; 2514041; 2515041; 2517041; 2518041; 2519041; 2520041; 2521041; 2522041; 2524041; 2525041; 2526041
lot2520041510041; 2511041; 2512041; 2513041; 2514041; 2515041; 2517041; 2518041; 2519041; 2520041; 2521041; 2522041; 2524041; 2525041; 2526041
lot2521041511041; 2512041; 2513041; 2514041; 2515041; 2517041; 2518041; 2519041; 2520041; 2521041; 2522041; 2524041; 2525041; 2526041
lot252204112041; 2513041; 2514041; 2515041; 2517041; 2518041; 2519041; 2520041; 2521041; 2522041; 2524041; 2525041; 2526041
lot252404113041; 2514041; 2515041; 2517041; 2518041; 2519041; 2520041; 2521041; 2522041; 2524041; 2525041; 2526041
lot252504114041; 2515041; 2517041; 2518041; 2519041; 2520041; 2521041; 2522041; 2524041; 2525041; 2526041
lot252604115041; 2517041; 2518041; 2519041; 2520041; 2521041; 2522041; 2524041; 2525041; 2526041

Original FDA recall reason

Product has the potential to be contaminated with Listeria monocytogenes.

Recall details

Recall number
F-2344-2015
Event ID
71158
FDA status
Terminated
Initiated
May 1, 2015
Reported
Jun 3, 2015
Classified
May 28, 2015
Terminated
Jul 28, 2015
Quantity
11,129
Location
Brampton, Canada
Initiation type
Voluntary: Firm initiated
Notification
Press Release

Where it was distributed

Domestic: IL, IN, KY, MI, MN, MO, ND, OH, WI and WV through retail stores, distributors and food service establishments. DOD/VA: None

FDA source record · F-2344-2015

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

Follow official FDA and manufacturer guidance.