Failed Tablet/Capsule Specification: some capsules over time do not meet or are suspected to not meet the specification for acid resistance.
Failed Tablet/Capsule Specification: some capsules over time do not meet or are suspected to not meet the specification for acid resistance.
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 Kremers Urban Pharmaceuticals, Inc. to request your refund or repair — edit it as you like.
Subject: Recall D-009-2014 — Kremers Urban Pharmaceuticals, Inc. Kremers Urban Pharmaceuticals, Inc. recalls Omeprazole Delayed-R Hello, I own a Kremers Urban Pharmaceuticals, Inc. recalls Omeprazole Delayed-Release Capsules, USP, 20 mg, Rx Only, 1000 Capsules per bottle, Distributed by: Kremers Urban that is covered by recall D-009-2014 from Kremers Urban Pharmaceuticals, 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.
