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Integra® Pole Mount External CSF Drainage System

Integra Lifesciences Corporation · Model SP0205 · UDI-DI 10381780071990

JXG Prescription
1
510(k) clearances
25,520
Adverse events (222 deaths)
108
Recalls
70
Facilities

Description

The External CSF Drainage Systems provide a sterile fluid path resistant to microbial particles. The systems are used to drain cerebrospinal fluid (CSF) from the ventricles of the brain of the lumbar subarachnoid space to a drainage bag. System components facilitate CSF drainage, fluid injection, CSF sampling and intracranial pressure (ICP) monitoring.

Recalls

DateFirmReason
2026-04-10Integra LifeSciences Corp. (NeuroSciences)Out-of-specification endotoxin result that did not meet the acceptance criteria.
2024-12-16Integra LifeSciences Corp.Potential for certain SKUs and lot numbers were distributed with the incorrect product description on the internal and external labels.
2024-12-16Integra LifeSciences Corp.Potential for certain SKUs and lot numbers were distributed with the incorrect product description on the internal and external labels.
2024-12-16Integra LifeSciences Corp.Potential for certain SKUs and lot numbers were distributed with the incorrect product description on the internal and external labels.
2024-05-07Integra LifeSciences Corp.Defect in the external sterile packaging (pouch) leading to a gap or/and weakness of the seal may compromise the product sterility.
2024-05-07Integra LifeSciences Corp.Defect in the external sterile packaging (pouch) leading to a gap or/and weakness of the seal may compromise the product sterility.
2024-05-07Integra LifeSciences Corp.Defect in the external sterile packaging (pouch) leading to a gap or/and weakness of the seal that may compromise the product sterility.
2023-11-28Natus Medical IncorporatedSterility assurance cannot be guaranteed for external drainage systems due to incomplete bioburden testing.
2023-11-28Natus Medical IncorporatedSterility assurance cannot be guaranteed for external drainage systems due to incomplete bioburden testing.
2023-06-28Medtronic NeurosurgeryProduct labeling contains incorrect expiration date

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.