Failed Dissolution Specifications: Product is being recalled due to out of specification dissolution results obtained during routine stability testing.
Failed Dissolution Specifications: Product is being recalled due to out of specification dissolution results obtained during routine stability testing.
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 Teva Pharmaceuticals USA, Inc to request your refund or repair — edit it as you like.
Subject: Recall D-848-2013 — Teva Pharmaceuticals USA, Inc Teva Pharmaceuticals USA, Inc. recalls Methylphenidate Hydrochloride E Hello, I own a Teva Pharmaceuticals USA, Inc. recalls Methylphenidate Hydrochloride Extended-Release Capsules (LA), 30 mg, 100 count bottle, Rx only, TEVA PHARMACEUTICALS that is covered by recall D-848-2013 from Teva Pharmaceuticals USA, 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.
