Shimadzu Trinias DAP Meter Recall: Out of Tolerance Risk
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.
Lower-risk recall
The DAP meters were found to be outside of tolerance.
Contact the company
What happened, in plain English
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. Read more at govinfonow.com/recall/66575-shimadzu-trinias-dap-meter-recall-out-of-tolerance-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/66575-shimadzu-trinias-dap-meter-recall-out-of-tolerance-risk · Updated August 19, 2026 · FDA enforcement record: FDA #Z-2591-2020
Cite this page
“Shimadzu Trinias DAP Meter Recall: Out of Tolerance Risk.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/66575-shimadzu-trinias-dap-meter-recall-out-of-tolerance-risk. Based on FDA recall #Z-2591-2020 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2591-2020%22&limit=1).
Why it’s dangerous
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.
Who’s affected
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.
How to tell if you have this one
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.
- Brand
Shimadzu Medical Systems- Category
Medical device
What to do — step by step
Check Serial Numbers
Identify if your Trinias DAP meter has serial numbers LR051A58B027, LR051A58B028, or LR051A58B029.
Where it went and when
Where it was distributed
Distributed nationwide and abroad; the notice names 3 states.
FDA distribution: “US Nationwide distribution including in the states of FL, KY, and LA. There was no government/military/foreign distribution.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Named in the notice: Florida, Kentucky, Louisiana.
Recall timeline
FDA published this recall 9 months after the firm started it.
- Firm started the recall
- FDA classified it Class II
- Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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Where this comes from
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.
- Official source: FDA Recall #Z-2591-2020 (November 4, 2019) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2591-2020 to see it in context.
- Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.