Class ITerminated in FDA datasetJun 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.

Check the codes ↓

The exact product

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

Check the codes

Compare these FDA-provided codes, lot numbers or dates with the product you have.

Match the product, size and code together. A similar name alone does not identify your batch.

Original FDA code information

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

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

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 ↗

A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.