Amgen recalls Corlanor 5mg tablets (NDC 55513-800-99 and 55513-800-60) due to foreign substance presence. Rx-only medication with specific lot numbers and expiration dates.
Presence of Foreign Substance.
Amgen is recalling Corlanor 5mg tablets because they contain a foreign substance. This could pose a risk to users, though the exact nature of the foreign substance isn't specified in the recall notice.
The presence of a foreign substance in the tablets could potentially cause harm when taken by patients. However, the recall notice does not specify what the foreign substance is or how it could cause injury.
People who have prescription Corlanor 5mg tablets from Amgen, specifically those with the listed lot numbers and expiration dates. Patients taking this medication for heart conditions are most at risk.
Check your Corlanor 5mg tablets for the following lot numbers: 1138901, 1149846, 1138201, 1138202, 1138900, 1141143, 1140280, 1140281, 1142063, 1142062, 1142942, 1142943, 1144081, 1144104, 1146373, 1146374, 1147491, 1147492, 1149843, 1151113, 1151890, 1153401, 1151114, 1151115, 1152412, 1153399, 1153400, 1155834, 1155835, 1155836, 1158480, 1158481, 1158482, 1160354, 1160355, 1161593, 1161594, 1161595, 1164097, 1164098, 1164099, 1165078, 1165079, 1165080, 1168005, 1168006, 1168007, 1169288, 1169289, 1172885. These tablets were made in Italy and have specific expiration dates.
Look for the lot numbers listed in the recall notice to determine if your Corlanor tablets are affected.
The recall notice does not specify what the foreign substance is.
Check the lot numbers listed in the recall notice, which include specific numbers and expiration dates.
The recall notice does not provide a remedy, so there is no specific action required beyond checking the lot numbers.
We’ve drafted a message you can send Amgen to request your refund or repair — edit it as you like.
Subject: Recall D-0612-2026 — Amgen Amgen Hello, I own a Amgen that is covered by recall D-0612-2026 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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