Natus recalls OBM DAB digital acquisition boxes with backward electrode labels that could cause misdiagnosis of neonatal seizures. Affected units have serial numbers starting with OBM. Contact Natus for details.
Electrode placement labels on the Digital Acquisition Box (DAB) were applied backwards. This may ultimately lead to misdiagnosis of seizure location in neonates monitored with this device.
Natus is recalling digital acquisition boxes used for neonatal seizure monitoring because electrode labels were applied backwards. This could lead to misdiagnosis of seizure locations in newborns. The recall affects specific model units with serial numbers starting with OBM.
The electrode placement labels on the device were applied incorrectly. This could cause the device to misdiagnose the location of seizures in newborns, potentially leading to inappropriate treatment decisions.
Neonatal care providers using the OBM DAB digital acquisition box for seizure monitoring are most at risk. The recall applies to units with serial numbers starting with OBM.
Check the serial number on your OBM DAB device. Affected units have serial numbers starting with 'OBM' followed by a sequence of numbers (e.g., OBM00002H3613).
Look for a serial number starting with 'OBM' on the device.
The recalled device is the OBM DAB (Digital Acquisition Box) with serial numbers starting with 'OBM'.
Check the serial number on your device; affected units start with 'OBM' followed by a sequence of numbers.
The recall does not specify a remedy, so contact Natus Neurology directly for guidance.
We’ve drafted a message you can send Natus Neurology to request your refund or repair — edit it as you like.
Subject: Recall Z-1925-2025 — Natus Neurology Natus Neurology Hello, I own a Natus Neurology that is covered by recall Z-1925-2025 from Natus Neurology. 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.
