Presence of Foreign Substance: Tablets are being recalled due to gray defects identified in the tablets.
Presence of Foreign Substance: Tablets are being recalled due to gray defects identified in the tablets.
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-149-2013 — West-Ward Pharmaceutical Corp. West-ward Pharmaceutical Corp. recalls PredniSONE Tablets, USP, 10 mg Hello, I own a West-ward Pharmaceutical Corp. recalls PredniSONE Tablets, USP, 10 mg, packaged in a) 100-count tablets per bottle (NDC 0143-1473-01), b) 1000-count tablets that is covered by recall D-149-2013 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.
