Class IITerminated in FDA datasetRecall initiated Mar 28, 2023

Zone Perfect Fudge Graham bar 50g bars packaged in foil wrapped- 12 bars individually wrapped…

Recalling firm: Abbott Laboratories

Why it was recalled

Potential of foreign material (hard plastic) within 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: Dec 14, 2023.

Check your package

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

ProductZone Perfect Fudge Graham bar 50g bars packaged in foil wrapped- 12 bars individually wrapped per cardboard carton
Package size50g

FDA code information

Lot No - 47961B800 List No - 63259 Expiration Date 03/01/24 Display Lot No - 49012SQoo Display List No - 64138

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

Full FDA record and distribution details

Original product description

Zone Perfect Fudge Graham bar 50g bars packaged in foil wrapped- 12 bars individually wrapped per cardboard carton

Extracted codes and context

TypeCode / valueContext
expiration03/01/24Lot No - 47961B800 List No - 63259 Expiration Date 03/01/24 Display Lot No - 49012SQoo Display List No - 64138

Original FDA recall reason

Potential of foreign material (hard plastic) within product

Recall details

Recall number
F-0698-2023
Event ID
92015
FDA status
Terminated
Initiated
Mar 28, 2023
Reported
Apr 19, 2023
Classified
Apr 7, 2023
Terminated
Dec 14, 2023
Quantity
646,668 bars
Location
Columbus, OH, 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

AL, AZ, CA, CO, CT, FL, GA, IA, ID, IL, IN, KS, LA, MA, MD, ME, MI, MN, MO, NC, NE, NJ, NV, NY, OH, PA, SC, SD, TN, TX, UT, VA, WA, WI, WV

FDA source record · F-0698-2023

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

Follow official FDA and manufacturer guidance.