Beckman Coulter recalls iQ200 Series Urine Microscopy Analyzers with NFT-2100 barcode readers that may fail to read urine sample barcodes, causing incorrect results that could delay treatment for conditions like hematuria.
iQ200 Series Urine Microscopy Analyzer may intermittently fail to read urine sample dilution barcode labels causing erroneous results that could delay treatment for health conditions such as hematuria.
Beckman Coulter is recalling iQ200 Series Urine Microscopy Analyzers with NFT-2100 barcode readers because they may fail to read urine sample dilution barcodes, leading to incorrect test results that could delay treatment for health issues such as blood in urine. This affects users who rely on these devices for accurate urine analysis.
The device may intermittently fail to read urine sample dilution barcode labels, which can cause the test to produce incorrect results. This could lead to delays in treating health conditions such as hematuria (blood in urine) if the incorrect results are not recognized.
Users of Beckman Coulter iQ200 Series Urine Microscopy Analyzers with NFT-2100 barcode readers who perform urine tests at home or in clinical settings. Those who rely on accurate urine test results for health monitoring are most at risk.
Check if your device has the model NFT-2100 barcode reader and catalog numbers listed in the recall notice (800-3046 to 800-3937, etc.). All iQ200 Series units with this specific barcode reader are affected.
Verify if your device has the NFT-2100 barcode reader model and catalog numbers listed in the recall notice.
Reach out to Beckman Coulter for guidance on next steps if you own an affected device.
The iQ200 Series Urine Microscopy Analyzer with NFT-2100 barcode reader may intermittently fail to read urine sample dilution barcodes, causing incorrect test results that could delay treatment for health conditions like hematuria.
Catalog numbers 800-3046, 800-3047, 800-3052, and other numbers listed in the recall notice (800-3042 to 800-3937, etc.).
No, the recall does not require immediate discontinuation. Affected users should check their device model and contact Beckman Coulter for guidance.
We’ve drafted a message you can send Beckman Coulter to request your refund or repair — edit it as you like.
Subject: Recall Z-1366-2018 — Beckman Coulter Beckman Coulter Hello, I own a Beckman Coulter that is covered by recall Z-1366-2018 from Beckman Coulter. 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.
