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Lower risk Food recall · FDA · Published March 28, 2023

Abbott Zone Perfect Fudge Graham Bars Recall: Foreign Material Hazard

Abbott recalls Zone Perfect Fudge Graham bars due to potential hard plastic foreign material. Consumers should check lot numbers on packaging for affected items.

🇺🇸 FDA recall #F-0698-2023FoodAbbott Laboratories ›
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Recalling firmAbbott Laboratories2900 Easton Square Pl · Columbus, OH 43219-6225
✎ GovInfoNow plain-language explainer

Abbott is recalling Zone Perfect Fudge Graham bars that may contain hard plastic pieces. This could cause injury if swallowed or ingested. Read more at govinfonow.com/recall/11306-abbott-zone-perfect-fudge-graham-bars-recall-foreign-material-hazard.

Source Summary by GovInfoNow · govinfonow.com/recall/11306-abbott-zone-perfect-fudge-graham-bars-recall-foreign-material-hazard · Updated September 23, 2026 · FDA enforcement record: FDA #F-0698-2023

Cite this page

“Abbott Zone Perfect Fudge Graham Bars Recall: Foreign Material Hazard.” GovInfoNow, updated September 23, 2026. https://govinfonow.com/recall/11306-abbott-zone-perfect-fudge-graham-bars-recall-foreign-material-hazard. Based on FDA recall #F-0698-2023 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0698-2023%22&limit=1).

The FDA announced on March 28, 2023, that Abbott Laboratories voluntarily recalled Zone Perfect Fudge Graham bars due to the potential for hard plastic foreign material. The recall affects 646,668 bars distributed across 33 states.

How to tell if you have it

  • Brand: Abbott Laboratories
  • Product: Zone Perfect Fudge Graham bar 50g bars packaged in foil wrapped- 12 bars individually wrapped per cardboard carton
  • Lot No: 47961B800
  • List No: 63259
  • Expiration Date: 03/01/24
  • Display Lot No: 49012SQoo
  • Display List No: 64138

The hazard

The product contains the potential for foreign material, specifically hard plastic. The FDA classified this as a Class II recall.

Context

GovInfoNow's records show Abbott Laboratories has 33 other recalls on record since May 14, 2012. Recent Abbott recalls include an Alinity ci-series System Control Module correction on November 13, 2025, and a software issue for the hq analyzer reported on September 18, 2025. Other recent recalls of similar products include Dreyer's Grand Outshine Fruit Bars Recall (August 18, 2026) and Gifford's POWER PLAY FUDGE Ice Cream Recall (August 14, 2026).

How to tell if you have this one

Check the lot number on the packaging: 47961B800 or 49012SQoo. The bars are 50g each, packaged in foil with 12 bars per cardboard carton.

  • Brand
    Abbott Laboratories
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Packaging

    Look for lot numbers 47961B800 or 49012SQoo on the packaging.

Where it went and when

Where it was distributed

Distributed in 35 states.

Alaska: not listedAKMaine: yesMEVermont: not listedVTNew Hampshire: not listedNHWashington: yesWAIdaho: yesIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: not listedRIMassachusetts: yesMAOregon: not listedORNevada: yesNVWyoming: not listedWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: not listedKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: not listedDEArizona: yesAZNew Mexico: not listedNMKansas: yesKSArkansas: not listedARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: yesLAMississippi: not listedMSAlabama: yesALGeorgia: yesGAHawaii: not listedHITexas: yesTXFlorida: yesFL

FDA 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” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Alabama, Arizona, California, Colorado, Connecticut, Florida, Georgia, Idaho, Illinois, Indiana, Iowa, Kansas, Louisiana, Maine, Maryland, Massachusetts, Michigan, Minnesota, Missouri, Nebraska, Nevada, New Jersey, New York, North Carolina, Ohio, Pennsylvania, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, West Virginia, Wisconsin.

Recall timeline

FDA terminated this recall 9 months after the firm started it.

1. Firm started the recall: Mar 28, 202312. FDA classified it Class II: Apr 7, 202323. Published in FDA’s Enforcement Report: Apr 19, 202334. FDA terminated the recall: Dec 14, 202342023
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

✎ GovInfoNow

Questions people ask

What should I do if I have the recalled bars?

Check the lot number on the packaging. If it matches, contact Abbott Laboratories for further instructions.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #F-0698-2023 (March 28, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0698-2023 to see it in context.
  • Plain-language summary written by qwen3:4b on September 23, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA