Failed impurities/ degradation specifications: Product is Out of Specification for an unspecified degradation product.
Failed impurities/ degradation specifications: Product is Out of Specification for an unspecified degradation product.
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 Upsher Smith Laboratories, Inc. to request your refund or repair — edit it as you like.
Subject: Recall D-0281-2019 — Upsher Smith Laboratories, Inc. Upsher Smith Laboratories, Inc. recalls Bumetanide Tablets, USP, 2 Hello, I own a Upsher Smith Laboratories, Inc. recalls Bumetanide Tablets, USP, 2 mg, 100-count bottle, Rx only, Manufactured by: Upser-Smith Laboratories, LLC, Maple Grove, that is covered by recall D-0281-2019 from Upsher Smith Laboratories, 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.
