Defective Delivery System; reports of damaged product that may alter the predicted release of scopolamine following transdermal application.
Defective Delivery System; reports of damaged product that may alter the predicted release of scopolamine following transdermal application.
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 Sandoz Inc to request your refund or repair — edit it as you like.
Subject: Recall D-0133-2017 — Sandoz Inc Sandoz Inc recalls Transderm Scop (scopolamine) Transdermal System, 1.5 mg, 24 patches M Hello, I own a Sandoz Inc recalls Transderm Scop (scopolamine) Transdermal System, 1.5 mg, 24 patches Multi pack, Rx only, Marketed by Baxter Healthcare that is covered by recall D-0133-2017 from Sandoz Inc. 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.
