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Use caution Drug recall · FDA · Published July 18, 2012

Walgreens Aspirin Free Tension Headache Recall: Undeclared Sucralose

Walgreens recalls specific lots of Aspirin Free Tension Headache caplets due to undeclared sucralose. Check your bottle's lot number and expiration date.

🇺🇸 FDA recall #D-0319-2015DrugWalgreens ›
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Recalling firmLNK International, Inc.40 & 60 Arkay Drive · Hauppauge, NY 11788-3708
✎ GovInfoNow plain-language explainer

LNK International, Inc. is recalling specific lots of Walgreens brand Aspirin Free Tension Headache Caplets because the label did not declare the presence of sucralose. This affects approximately 9,379 bottles distributed nationwide. The recall was initiated on July 18, 2012. Read more at govinfonow.com/recall/48626-lnk-international-inc-recalls-walgreens-aspirin-free-tension-headache-pain.

Source Summary by GovInfoNow · govinfonow.com/recall/48626-lnk-international-inc-recalls-walgreens-aspirin-free-tension-headache-pain · Updated October 13, 2026 · FDA enforcement record: FDA #D-0319-2015

Cite this page

“Walgreens Aspirin Free Tension Headache Recall: Undeclared Sucralose.” GovInfoNow, updated October 13, 2026. https://govinfonow.com/recall/48626-lnk-international-inc-recalls-walgreens-aspirin-free-tension-headache-pain. Based on FDA recall #D-0319-2015 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0319-2015%22&limit=1).

The FDA announced on July 18, 2012, that LNK International, Inc. recalled Walgreens brand Aspirin Free Tension Headache Caplets due to undeclared sucralose. The recall affects specific lots distributed nationwide.

How to tell if you have it

  • Walgreens ASPIRIN FREE TENSION HEADACHE, Pain Reliever/Pain Reliever Aid, Acetaminophen & Caffeine, 100 Coated Caplets
  • UPC Code 311917134925
  • Lot Number P78221, expiration date 05/14
  • Lot Number P78222, expiration date 05/14

The hazard

The firm recalled specific lots of Walgreens brand Aspirin Free Tension Headache Caplets due to the presence of sucralose, which was not declared on the label.

Context

GovInfoNow's records show LNK International, Inc. has 5 other recalls on record since 2019-07-10. Other recent recalls include a Kirkland Severe Cold & Flu recall for CGMP deviations (2024-11-14), an LNK Walgreens Sinus Relief product mislabeled as decongestant-free (2022-10-11), and LNK Nighttime Sleep-Aid Tablets with incorrect labeling risk (2022-08-04). Other recent recalls of similar products include a Walgreens Saline Nasal Spray with Xylitol recall for microbial contamination risk (2025-11-12), an Xyvona (Levorphanol) 2mg Tablet recall due to FDA denial of marketing (2026-05-22), and a Sun Pharmaceutical Fluocinolone Acetonide Solution recall for impurity risk (2025-12-30).

How to tell if you have this one

Check your bottle for Item # 427594, NDC 0363-0428-12, and UPC Code 311917134925. The recall applies to Lot Number P78221 and Lot Number P78222, both with an expiration date of 05/14.

  • Brand
    Walgreens
  • Product
    Walgreens ASPIRIN FREE TENSION HEADACHE, Pain Reliever/Pain Reliever Aid, Acetaminophen & Caffeine, 100 Coated Caplets
  • Category
    Drug

Where it went and when

Where it was distributed

Distributed nationwide.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

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

Distributed nationwide.

Recall timeline

FDA terminated this recall 2.4 years after the firm started it.

1. Firm started the recall: Jul 18, 201212. FDA classified it Class II: Dec 23, 201423. FDA terminated the recall: Dec 23, 201434. Published in FDA’s Enforcement Report: Dec 31, 2014420122014
  1. Firm started the recall
  2. FDA classified it Class II
  3. FDA terminated the recall
  4. Published in FDA’s Enforcement Report

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 #D-0319-2015 (July 18, 2012) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0319-2015 to see it in context.
  • Plain-language summary written by qwen3.6:35b-a3b on October 13, 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