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Unrated Food recall · FDA · Published August 2, 2019

Lipt: Diet Peach Iced Tea Bottles with Undeclared Ingredients Recalled

Lipton Diet Peach Iced Tea bottles from Pepsi/Lipton Partnership contain undeclared Malic Acid and Citrus Pectin. Consumers should check labels for specific batch codes to determine if affected.

🇺🇸 FDA recall #F-2095-2019FoodLipton ›
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Contact the company

Recalling firmPepsi Bottling Ventures, LLC1900 Pepsi Way · Garner, NC 27529-7232
✎ GovInfoNow plain-language explainer

Lipton Diet Peach Iced Tea bottles produced by independent producers for Pepsi/Lipton Partnership are being recalled because they contain undeclared Malic Acid and Citrus Pectin. This could pose a risk to consumers who have these bottles. Read more at govinfonow.com/recall/16783-lipt-diet-peach-iced-tea-bottles-with-undeclared-ingredients-recalled.

Source Summary by GovInfoNow · govinfonow.com/recall/16783-lipt-diet-peach-iced-tea-bottles-with-undeclared-ingredients-recalled · Updated October 5, 2026 · FDA enforcement record: FDA #F-2095-2019

Cite this page

“Lipt: Diet Peach Iced Tea Bottles with Undeclared Ingredients Recalled.” GovInfoNow, updated October 5, 2026. https://govinfonow.com/recall/16783-lipt-diet-peach-iced-tea-bottles-with-undeclared-ingredients-recalled. Based on FDA recall #F-2095-2019 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2095-2019%22&limit=1).

The FDA announced on August 2, 2019, that Pepsi Bottling Ventures, LLC voluntarily recalled Lipton Diet Iced Tea Peach bottles due to undeclared Malic Acid and Citrus Pectin allergens. The firm placed peach tea labels on diet peach tea bottles, creating a potential allergic reaction hazard for consumers.

How to tell if you have it

  • Brand: Lipton
  • Product: Lipton DIET ICED TEA PEACH 6/16.9 oz plastic bottles
  • Manufacturer: Independent producers for the Pepsi/Lipton Tea Partnership
  • Best Taste Limit and Production Codes: NOV0419 1845 GC 070395 to NOV 0419 1915 GC 070395
  • Distribution: Various customers in North Carolina

The hazard

The product contains undeclared Malic Acid and Citrus Pectin because Peach Tea Labels were placed on Diet Peach Tea bottles. The FDA classified this as a Class III recall, indicating the least dangerous category of recall, but no specific incidents or injuries were reported in the record.

Context

GovInfoNow's records show other recent recalls of similar products include Wawa Diet Iced Tea Lemon Pint Recall (2026-04-02) and Moonlight Packing Peppermint Peach Recall (2025-10-28). A second Moonlight Packing Peppermint Peaches Recall occurred on 2025-10-28.

How to tell if you have this one

Check for the batch codes on the bottle label: NOV0419 1845 GC 070395 to NOV 0419 1915 GC 070395. The product is a 6/16.9 oz plastic bottle with the Lipton Diet Peach Iced Tea name.

  • Brand
    Lipton
  • Category
    Food
Based on the official FDA remedy

What to do — step by step

  1. Check Bottle Label

    Look for the batch codes on the bottle label: NOV0419 1845 GC 070395 to NOV 0419 1915 GC 070395.

Where it went and when

Where it was distributed

Distributed in North Carolina.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: 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: yesNCSouth 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: “Product was shipped various customers in North Carolina.” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: North Carolina.

Recall timeline

FDA terminated this recall 6 months after the firm started it.

1. Firm started the recall: Aug 2, 201912. FDA classified it Class III: Aug 30, 201923. Published in FDA’s Enforcement Report: Sep 11, 201934. FDA terminated the recall: Feb 3, 2020420192020
  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.

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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-2095-2019 (August 2, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-2095-2019 to see it in context.
  • Plain-language summary written by qwen3:4b on October 5, 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