Shimadzu recalls digital angiography systems due to potential display abnormalities or no function from a capacitor manufacturing issue. Affected units have specific serial numbers.
Due to capacitor manufacturing issue, their is a potential that Flat Panel Device may have abnormal display or no function.
Shimadzu is recalling digital angiography systems that may have display problems or no function due to a capacitor issue. This could affect medical imaging equipment used in hospitals.
A manufacturing defect in the capacitor may cause the display to malfunction or stop working entirely. This could lead to incorrect imaging results or system unavailability during critical procedures.
Hospitals and medical facilities using Shimadzu digital angiography systems with the specified serial numbers are most at risk. Patients and staff using these systems could experience display issues.
Check for the serial number 41EFFF7D3001 or UDI (01)04540217058020 on the device. The product is a digital angiography system from Shimadzu.
Verify if the display is working properly or if the system has no function.
The recalled product is Shimadzu Digital Angiography System with serial number 41EFFF7D3001 or UDI (01)04540217058020.
The recall record does not mention a remedy or fix for this issue.
Check for the serial number 41EFFF7D3001 or UDI (01)04540217058020 on the device.
We’ve drafted a message you can send Shimadzu to request your refund or repair — edit it as you like.
Subject: Recall Z-1292-2024 — Shimadzu Shimadzu Hello, I own a Shimadzu that is covered by recall Z-1292-2024 from Shimadzu. 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.
