Zone Perfect Fudge Graham bar 50g bars packaged in foil wrapped- 12 bars individually wrapped per cardboard carton
Summary
The FDA issued a Class II for Zone Perfect Fudge Graham bar 50g bars packaged in foil wrapped- 12 bars individ by Abbott Laboratories. Reason: Potential of foreign material (hard plastic) within product.
Details
Source
Food Recall
External ID
F-0698-2023
Action Date
2023-04-19
Status
Terminated
Category
food
Product Description
Zone Perfect Fudge Graham bar 50g bars packaged in foil wrapped- 12 bars individually wrapped per cardboard carton
Lot/Code Info: Lot No - 47961B800 List No - 63259 Expiration Date 03/01/24 Display Lot No - 49012SQoo Display List No - 64138
Quantity Affected: 646,668 bars
Reason for Recall
Potential of foreign material (hard plastic) within product
Distribution
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
Type: Voluntary: Firm initiated
Recall Initiated: 2023-03-28
Company
Columbus, OH
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 45 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Abbott Laboratories has 101 FDA actions in our database, including 86 recalls and 15 clearances.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Abbott Laboratories) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Abbott Laboratories have FDA actions?
Abbott Laboratories has 101 FDA actions in our database, including 86 recalls and 15 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0698-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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