Presence of Particulate Matter: This product is being recalled due to the discovery of particles in the stability samples and retain samples.
Presence of Particulate Matter: This product is being recalled due to the discovery of particles in the stability samples and retain samples.
We break every recall down into plain English — this one’s still on our list. Until our write-up is ready, the official FDA hazard and remedy below have the full, accurate details.
We’ve drafted a message you can send West-Ward Pharmaceutical Corp. to request your refund or repair — edit it as you like.
Subject: Recall D-1438-2012 — West-Ward Pharmaceutical Corp. West-ward Pharmaceutical Corp. recalls Fosphenytoin Sodium Injection Hello, I own a West-ward Pharmaceutical Corp. recalls Fosphenytoin Sodium Injection, USP, 500 mg PE per 10 mL (50 mg PE per mL), 10 mL Single Dose Vial, packaged in 10-count that is covered by recall D-1438-2012 from West-Ward Pharmaceutical Corp.. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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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.
