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Unrated Drug recall · FDA · Published March 24, 2025

Amerisource Health Services recalls Voriconazole 50mg tablets due to repackaging issues

Amerisource Health Services is recalling Voriconazole 50mg tablets (30 doses per carton) because they were repackaged by a supplier, potentially affecting drug safety.

🇺🇸 FDA recall #D-0307-2025DrugAmerisource Health Services ›
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Recalling firmAmerisource Health Services LLC2550 John Glenn Ave Ste A · Columbus, OH 43217-1188
✎ GovInfoNow plain-language explainer

Amerisource Health Services is recalling Voriconazole 50mg tablets due to repackaging by a supplier. This recall is for safety reasons related to manufacturing practices. Read more at govinfonow.com/recall/32172-amerisource-health-services-recalls-voriconazole-50mg-tablets-due-to-repackaging.

Source Summary by GovInfoNow · govinfonow.com/recall/32172-amerisource-health-services-recalls-voriconazole-50mg-tablets-due-to-repackaging · Updated August 17, 2026 · FDA enforcement record: FDA #D-0307-2025

Cite this page

“Amerisource Health Services recalls Voriconazole 50mg tablets due to repackaging issues.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/32172-amerisource-health-services-recalls-voriconazole-50mg-tablets-due-to-repackaging. Based on FDA recall #D-0307-2025 (https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0307-2025%22&limit=1).

The FDA announced on March 24, 2025, that Amerisource Health Services LLC is recalling Voriconazole Tablets, 50 mg, due to current good manufacturing practice deviations. The company repackaged the product after receiving a request from its supplier.

How to tell if you have it

  • Brand: Amerisource Health Services
  • Product: Voriconazole Tablets, 50 mg
  • Packaging: Cartons of 3 blister cards with 10 individual blistered doses (30 Unit Dose per carton)
  • Distributed by: American Health Packaging, Columbus, Ohio 43217
  • Carton NDC: 60687-294-21
  • Unit Dose NDC: 60687-294-11
  • Lot #: 1014138
  • Expiration Date: 04/30/2025
  • Quantity: 889 cartons
  • Distribution: USA nationwide

The hazard

The recall is due to cGMP deviations because the company repackaged the product. This action was taken after notification from their supplier requesting the recall.

Context

GovInfoNow's records show Amerisource Health Services LLC has 30 other recalls on record since July 27, 2022. Recent brand recalls include a May 1, 2026, recall of Primidone Tablets for cross-contamination risk and a March 16, 2026, recall of Meclizine 12.5mg Tablets for failed tablet specifications. Other recent recalls of similar products include an Amneal recall of Primidone Tablets on June 3, 2026, and Golden State Medical recalls of Primidone Tablets on April 27, 2026.

How to tell if you have this one

Check for Voriconazole 50mg tablets in cartons with 30 doses (3 blister cards, 10 doses per card). Look for lot number 1014138 and expiration date 04/30/2025.

  • Brand
    Amerisource Health Services
  • Category
    Drug
Based on the official FDA remedy

What to do — step by step

  1. Check Product Details

    Verify the lot number and expiration date on the carton to confirm if it matches the recalled batch (lot #1014138, exp 04/30/2025).

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: “USA 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 11 months after the firm started it.

1. Firm started the recall: Mar 24, 202512. FDA classified it Class II: Mar 28, 202523. Published in FDA’s Enforcement Report: Apr 9, 202534. FDA terminated the recall: Feb 10, 2026420252026
  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.

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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-0307-2025 (March 24, 2025) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for D-0307-2025 to see it in context.
  • Plain-language summary written by qwen3:4b on August 17, 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