Fox Business92%
Nearly 1 million bottles of heart and kidney medication recalled over foreign substance found on tablets 11%
By Brie Stimson0%
6/28/2026, 3:00:52 AM
Topics: Pharmaceuticals, Public Health
BS Summary: This article contains 11 faulty reasoning types, including Framing Effect, Negativity Bias, and Ambiguity (Equivocation), with Appeal to Authority as the most egregious example at 35.9% saturation with 117 hits. Analysis detected 468 faulty-reasoning hits from 326 analyzed words, generating a BS Score of 27.5% and a BS Rank of 11% (19,629 of 21,887 articles). This article is better (less manipulative) than 89.70% of the article peer group.
Nearly one million bottles of heart and kidney medication have been recalled nationwide over the possibility of a "foreign substance," according to the U.S.
Food and Drug Administration.
California-based Amgen, Inc. voluntarily recalled at least 944,142 bottles of Corlanor and Sensipar tablets after "unexpected foreign matter" was found "in the reserve sample of one of the identified lots," the California state Board of Pharmacy said in an alert.
"The unexpected foreign matter was localized on the exterior tablet surface, over the coating," the board said.
"Therefore, as a precautionary measure, all lots within expiry that were processed in AML Building 23 packaging area, where the condition occurred, are being recalled."
The board added that hazard assessments have found it doesn’t present a clinical risk to patients and "overall patient safety risk is low."
There have been no complaints about the issue.
Corlanor, which is also known by the generic name ivabradine, is prescribed to treat patients with chronic heart failure and Sensipar, also known as cinacalcet hydrochloride, is mainly used to treat overactive parathyroidism in chronic kidney disease patients.
The tablets were distributed between Oct. 28, 2021 and Dec.
30, 2025.
The recall includes the following presentations, according to the board:
• Corlanor® (ivabradine) 5 mg, 60 tablets in 1 bottle; NDC 55513-800-60
• Corlanor® (ivabradine) 5 mg, 14 tablets in 1 bottle; NDC 55513-800-99
• Corlanor® (ivabradine) 5 mg, 60 tablets in 1 bottle; NDC 55513-810-60
• Sensipar® (cinacalcet hydrochloride) 30 mg, 30 tablets in 1 bottle; NDC 55513-073- 30
• Sensipar® (cinacalcet hydrochloride) 60 mg, 30 tablets in 1 bottle; NDC 55513-074- 30
• Sensipar® (cinacalcet hydrochloride) 90 mg, 30 tablets in 1 bottle; NDC 55513-075- 30
The FDA has characterized the recall as Class II, meaning it could "cause temporary or medically reversible adverse health consequences or where the probability of serious adverse health consequences is remote."
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100%flagged-word coverageCalifornia state Board of Pharmacy
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