Amgen recalls 90mg Sensipar tablets with CGMP deviations; affected lots may pose quality risks. Consumers should check NDC and expiration dates for affected products.
CGMP Deviations
Amgen is recalling 90mg Sensipar tablets that were manufactured with CGMP deviations. This recall is for safety reasons related to potential quality issues in the product.
CGMP deviations refer to manufacturing process issues that could affect product quality. While the specific risk isn't detailed, such deviations may lead to potential quality concerns in the medication.
Prescription holders of Sensipar 90mg tablets with NDC 55513-075-30 and lot number 1157056. Patients on calcium regulation therapy are most at risk.
Check for NDC code 55513-075-30 and lot number 1157056 on the product label. The expiration date is February 29, 2028.
Look for NDC code 55513-075-30 and lot number 1157056 on the tablet packaging.
The recall is due to CGMP deviations, but Amgen has not specified if the product is unsafe. Consumers should check the label for the affected lot number.
Check for NDC code 55513-075-30 and lot number 1157056 on the product label. The expiration date is February 29, 2028.
The recall does not specify a remedy, so consumers should check the product label and contact Amgen for further instructions.
We’ve drafted a message you can send Amgen to request your refund or repair — edit it as you like.
Subject: Recall D-0616-2026 — Amgen Amgen Hello, I own a Amgen that is covered by recall D-0616-2026 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.
