Ref: NT821731C, Natus EDS 3 CSF External Drainage System - Product Usage: indicated for draining cerebrospinal fluid (CFS) from the cerebral ventricles or the lumbar subarachnoid space as a means of reducing intracranial pressure and CSF volume when the insertion of a permanent, internal shunt is not indicated.
FDA Recall Z-1143-2021 · Posted None
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Recalling FirmNatus Manufacturing Limited
Recall StatusTerminated
Product CodeJXG
Date Initiated2021-01-12
Date Terminated2022-11-08
Product Quantity7 units
Reason for Recall
The external drainage system failed to meet Pyrogen test requirements for devices contacting cerebrospinal fluid of 2.15 endotoxins.
Firm Action
On January 12, 2021, Natus sent an "Urgent Field Safety Notice - Recall" notification to all affected consignees via US Mail. In addition to informing consignees about the recall, the notification asked consignees to take the following actions:
1. Please return these affected items at your earliest convenience to the following address: 3150 Pleasant View Road, Middleton, WI 53562 USA
2. Replacement product is available. The Technical Service department will be in contact in relation to the provision of the replacement product.
3. Please complete and return the customer reply form to Natus at the following Email address: [email protected]
Root Cause
Release of Material/Component prior to receiving test results
Distribution Pattern
US Nationwide distribution in the state of NY.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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