Amgen recalls 30mg Sensipar tablets with CGMP deviations. This prescription medication may have quality issues affecting safety. Consumers should contact Amgen for details.
CGMP Deviations
Amgen is recalling 30mg Sensipar tablets that were manufactured in Japan and distributed by Amgen. The recall is due to manufacturing deviations that could affect product safety.
The recall is for manufacturing deviations that could affect product safety. CGMP deviations refer to quality control issues during production that may impact the medication's safety and effectiveness.
Prescription medication users who have the specific 30mg Sensipar tablets with NDC 55513-073-30 and lot number 1156858. People taking calcium regulation treatment are most at risk.
Check for Sensipar 30mg tablets with NDC code 55513-073-30 and lot number 1156858. These tablets were manufactured in Japan and distributed by Amgen in Thousand Oaks, CA.
Reach out to Amgen directly for specific recall instructions and assistance with the product.
The recall is due to manufacturing deviations that could affect safety, so it is not recommended to use these specific tablets.
Look for Sensipar 30mg tablets with NDC 55513-073-30 and lot number 1156858, which were manufactured in Japan and distributed by Amgen in Thousand Oaks, CA.
Contact Amgen directly for specific instructions on how to handle the product.
We’ve drafted a message you can send Amgen to request your refund or repair — edit it as you like.
Subject: Recall D-0613-2026 — Amgen Amgen Hello, I own a Amgen that is covered by recall D-0613-2026 from Amgen. 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.
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