Skip to content
Use caution Food recall · FDA · Published July 13, 2018

Diet Pepsi 7.5 oz Recall: Undeclared Aspartame in 6-Packs

PepsiCo recalls Diet Pepsi 7.5 oz 6-packs due to undeclared aspartame. Check your UPC and use-by date for affected lots distributed in the Pacific Northwest.

🇺🇸 FDA recall #F-1731-2018FoodDiet Pepsi ›
Take action

Contact the company

Recalling firmPepsico Inc700 Anderson Hill Rd · Purchase, NY 10577-1401
✎ GovInfoNow plain-language explainer

What happened, in plain English

PepsiCo Inc is recalling Diet Pepsi 7.5 oz cans sold in 6-packs because they contain undeclared aspartame. This matters because individuals with phenylketonuria (PKU) must avoid aspartame to prevent serious health issues. The affected products were distributed in Alaska, Idaho, Montana, Oregon, and Washington. Read more at govinfonow.com/recall/18984-diet-pepsi-7-5-oz-recall-undeclared-aspartame-in-6.

Source Summary by GovInfoNow · govinfonow.com/recall/18984-diet-pepsi-7-5-oz-recall-undeclared-aspartame-in-6 · Updated October 11, 2026 · FDA enforcement record: FDA #F-1731-2018

Cite this page

“Diet Pepsi 7.5 oz Recall: Undeclared Aspartame in 6-Packs.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/18984-diet-pepsi-7-5-oz-recall-undeclared-aspartame-in-6. Based on FDA recall #F-1731-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1731-2018%22&limit=1).

Why it’s dangerous

The product contains aspartame, an artificial sweetener that is not listed on the ingredient label. For people with PKU, consuming aspartame can lead to elevated levels of phenylalanine in the blood and brain, which can cause serious health problems.

Who’s affected

Consumers who purchased the recalled Diet Pepsi 7.5 oz 6-packs in Alaska, Idaho, Montana, Oregon, or Washington are affected. Individuals with phenylketonuria (PKU) are at risk due to the undeclared aspartame.

How to tell if you have this one

Look for Diet Pepsi 7.5 oz cans sold in 6-packs. Check the case label for UPC 0 12000 16314 2. Verify the lot number (XXX TT051081 with Use By Date AUG 20 18, or XXX TT060581 with Use By Date SEP 17 18).

  • Brand
    Diet Pepsi
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Your Product Details

    Verify if your Diet Pepsi 7.5 oz 6-pack matches the UPC 0 12000 16314 2 and lot numbers XXX TT051081 or XXX TT060581.

  2. Contact PepsiCo for Remedy

    The recall record does not specify a remedy, so contact PepsiCo directly for instructions on returns or refunds.

Where it went and when

Where it was distributed

Distributed in 5 states.

Alaska: yesAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: yesORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: not listedTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: not listedALGeorgia: not listedGAHawaii: not listedHITexas: not listedTXFlorida: not listedFL

FDA distribution: “distributed in AK, ID, MT, OR, and WA” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Alaska, Idaho, Montana, Oregon, Washington.

Recall timeline

FDA terminated this recall 3 months after the firm started it.

1. Firm started the recall: Jul 13, 201812. FDA classified it Class III: Aug 2, 201823. Published in FDA’s Enforcement Report: Aug 8, 201834. FDA terminated the recall: Oct 24, 201842018
  1. Firm started the recall
  2. FDA classified it Class III
  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.

Similar recalls

Latest food recalls

Keep exploring

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-1731-2018 (July 13, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1731-2018 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 11, 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