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Stop using now Food recall · FDA · Published May 25, 2018

Watan Dried Apricot Recall: Undeclared Sulfites Hazard

Global Commodities Inc recalls Watan dried apricots due to undeclared sulfites. Check your pantry for affected lots from Pakistan.

🇺🇸 FDA recall #F-1565-2018FoodWatan ›
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Recalling firmGlobal Commodities Inc122 New South Rd · Hicksville, NY 11801-5263
✎ GovInfoNow plain-language explainer

What happened, in plain English

Global Commodities Inc is recalling Watan brand dried apricots because they contain high levels of undeclared sulfites (2901 ppm). This matters because sulfites can cause serious allergic reactions in sensitive individuals, particularly those with asthma. The product was produced in Pakistan and imported by Global Commodities Inc. Read more at govinfonow.com/recall/19095-watan-dried-apricot-recall-undeclared-sulfites-hazard.

Source Summary by GovInfoNow · govinfonow.com/recall/19095-watan-dried-apricot-recall-undeclared-sulfites-hazard · Updated October 11, 2026 · FDA enforcement record: FDA #F-1565-2018

Cite this page

“Watan Dried Apricot Recall: Undeclared Sulfites Hazard.” GovInfoNow, updated October 11, 2026. https://govinfonow.com/recall/19095-watan-dried-apricot-recall-undeclared-sulfites-hazard. Based on FDA recall #F-1565-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1565-2018%22&limit=1).

Why it’s dangerous

The product contains undeclared sulfites at a high concentration (2901 ppm). Sulfites are common preservatives that can trigger severe respiratory distress and other allergic symptoms in people who are sensitive to them, especially those with asthma.

Who’s affected

Consumers who purchased Watan Dried Apricot with Pitt, specifically the 1 LB and 0.50 LB packages. Individuals with sulfite allergies or asthma are at the highest risk of adverse reactions.

How to tell if you have this one

Look for Watan brand dried apricots labeled 'Premium Quality Natural Dried Apricot with Pitt.' Check the package size (1 LB or 0.50 LB), the origin ('Produce of Pakistan'), and the importer ('Global Commodities Inc, New York USA'). The best before date is December 2018.

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

What to do — step by step

  1. Stop consuming the product

    Do not eat the recalled dried apricots due to the risk of allergic reaction from undeclared sulfites.

  2. Check your packaging details

    Verify if you have the specific Watan brand product imported by Global Commodities Inc with a best before date of December 2018.

Where it went and when

Where it was distributed

Distributed in 8 states.

Alaska: not listedAKMaine: yesMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: not listedMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: not listedILWisconsin: not listedWIMichigan: not listedMINew York: yesNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: not listedPANew Jersey: yesNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: yesMOKentucky: not listedKYWest Virginia: not listedWVVirginia: yesVAMaryland: 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: yesGAHawaii: not listedHITexas: not listedTXFlorida: yesFL

FDA distribution: “VA, NY, VA, NC, MO, FL, GA, ME, NJ” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Florida, Georgia, Maine, Missouri, New Jersey, New York, North Carolina, Virginia.

Recall timeline

FDA terminated this recall 5 months after the firm started it.

1. Firm started the recall: May 25, 201812. FDA classified it Class I: Jun 13, 201823. Published in FDA’s Enforcement Report: Jun 13, 201834. FDA terminated the recall: Oct 11, 201842018
  1. Firm started the recall
  2. FDA classified it Class I
  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

Where was this product sold?

The record states the distribution pattern included Virginia, New York, North Carolina, Missouri, Florida, Georgia, Maine, and New Jersey.

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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-1565-2018 (May 25, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1565-2018 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