Brainlab recalls Curve navigation stations with specific model numbers due to incorrect calibration, which could lead to inaccurate measurements during medical procedures.
Incorrect manufacturer calibration
Brainlab is recalling specific models of their Curve navigation stations because they have incorrect calibration. This could cause inaccurate measurements during medical procedures, potentially affecting treatment outcomes.
The navigation stations have incorrect calibration, meaning they might provide inaccurate measurements during medical procedures. This could lead to improper treatment decisions if the measurements are not precise.
Medical professionals using Brainlab Curve navigation stations with the listed model numbers and serial codes are most at risk. Patients receiving procedures using these devices may also be affected.
Check for model numbers 19901, 19901B, 19900, or 19905 on the device. Look for specific serial numbers listed in the recall notice for each model.
Identify the model number on your Brainlab Curve device, which should be one of 19901, 19901B, 19900, or 19905.
Compare your device's serial number with the list provided in the recall notice to determine if it is affected.
The Brainlab Curve navigation stations have incorrect calibration, which could lead to inaccurate measurements during medical procedures.
Check the model number on your device (19901, 19901B, 19900, or 19905) and compare the serial number with the list provided in the recall notice.
The recall does not specify a remedy, so contact Brainlab directly for further instructions.
We’ve drafted a message you can send Brainlab to request your refund or repair — edit it as you like.
Subject: Recall Z-2792-2020 — Brainlab Brainlab Hello, I own a Brainlab that is covered by recall Z-2792-2020 from Brainlab. 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.
