Shimadzu recalls Trinias DAP meters (serials LR051A58B027-029) used in Digital Anglo System for medical procedures due to being outside tolerance. Affected users should contact Shimadzu for details.
The DAP meters were found to be outside of tolerance.
Shimadzu is recalling specific Trinias DAP meters used in their Digital Anglo System for medical procedures because they are outside tolerance. This could affect the accuracy of medical measurements during procedures like cardiology and radiology.
The DAP meters are outside tolerance, meaning they may not measure pressure accurately during medical procedures. This could lead to incorrect treatment decisions if used in critical procedures like cardiology or radiology.
Medical professionals using the Trinias DAP meters in the Digital Anglo System for procedures like cardiology and radiology. Those with serial numbers LR051A58B027, LR051A58B028, or LR051A58B029 are most at risk.
Check if your Trinias DAP meter has serial numbers LR051A58B027, LR051A58B028, or LR051A58B029. These meters are part of the Digital Anglo System used for interventional procedures.
Identify if your Trinias DAP meter has serial numbers LR051A58B027, LR051A58B028, or LR051A58B029.
The DAP meters are outside tolerance, which could lead to inaccurate pressure measurements during medical procedures.
Check if your Trinias DAP meter has serial numbers LR051A58B027, LR051A58B028, or LR051A58B029.
The recall record does not specify a remedy, so contact Shimadzu Medical Systems for further instructions.
We’ve drafted a message you can send Shimadzu Medical Systems to request your refund or repair — edit it as you like.
Subject: Recall Z-2591-2020 — Shimadzu Medical Systems Shimadzu Medical Systems Hello, I own a Shimadzu Medical Systems that is covered by recall Z-2591-2020 from Shimadzu Medical Systems. 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.
