Check the Batch
Class ITerminated in FDA datasetRecall initiated Jun 19, 2024

Terrafina, Macadamia in the Raw , Net Wt. 6oz , (170 g)

Recalling firm: SUNCO & FRENCHIE LLC.

Why it was recalled

Product tested positive for presence of salmonella.

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 8, 2024.

Check your package

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

ProductTerrafina, Macadamia in the Raw , Net Wt. 6oz , (170 g)
Package size6oz

FDA code information

ALL LOT NUMBERS AND QUANTITIES FROM BATCH # P43755.2 Lot# RMA241201, Lot# RMA241101, Lot# RMA231711, Lot# RMA231611, Lot # P43755.2

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

Full FDA record and distribution details

Original product description

Terrafina, Macadamia in the Raw , Net Wt. 6oz , (170 g)

Extracted codes and context

TypeCode / valueContext
batchP43755.2ALL LOT NUMBERS AND QUANTITIES FROM BATCH # P43755.2 Lot# RMA241201, Lot# RMA241101, Lot# RMA231711, Lot# RMA231611, Lot # P43755.2
lotP43755.255.2 Lot# RMA241201, Lot# RMA241101, Lot# RMA231711, Lot# RMA231611, Lot # P43755.2
lotRMA231611 FROM BATCH # P43755.2 Lot# RMA241201, Lot# RMA241101, Lot# RMA231711, Lot# RMA231611, Lot # P43755.2
lotRMA231711RS AND QUANTITIES FROM BATCH # P43755.2 Lot# RMA241201, Lot# RMA241101, Lot# RMA231711, Lot# RMA231611, Lot # P43755.2
lotRMA241101ALL LOT NUMBERS AND QUANTITIES FROM BATCH # P43755.2 Lot# RMA241201, Lot# RMA241101, Lot# RMA231711, Lot# RMA231611, Lot # P43755.2
lotRMA241201ALL LOT NUMBERS AND QUANTITIES FROM BATCH # P43755.2 Lot# RMA241201, Lot# RMA241101, Lot# RMA231711, Lot# RMA231611, Lot # P43755.2

Original FDA recall reason

Product tested positive for presence of salmonella.

Recall details

Recall number
F-1485-2024
Event ID
94906
FDA status
Terminated
Initiated
Jun 19, 2024
Reported
Jul 24, 2024
Classified
Jul 15, 2024
Terminated
Aug 8, 2024
Quantity
993.5 LBS
Location
Pine Brook, NJ, 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

The recalled product was distributed to NJ, NY

FDA source record · F-1485-2024

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

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