INFINITY DUAL HEMO MCable Pod
FDA Recall Z-0942-2018 · Posted None
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Recalling FirmDraegar Medical Systems, Inc.
Recall StatusTerminated
Product CodeMHX
Date Initiated2017-10-04
Date Terminated2018-06-15
Product Quantity2,760
Reason for Recall
Dual Hemo MCable Pods with Revision
Index (RI) 15 and 16, which are used with the Drger Infinity Acute Care System, may
permit liquid ingress inconsistent with their IPX4 rating, which could potentially result in an
incorrect measured value of invasive blood pressure.
Firm Action
In September of 2017 an Urgent medical Device Recall letter was issued to customers informing them of the recall and to request that inventory be checked to see if the product subject in the recall is on the premises. To do this, the customer will check the label for the revision index number which is located on the upper middle portion of label. RI number 15 and 16 are included in the recall. No other numbers are subject to recall. Affected product will receive a sleeve from the company to correct the issue. Questions or concerns can be directed to 1-800-437-2437 (Press 1, then press 32349) or contact Customer Care at 1-800-437-2437 (Press 4, then press 4 again)
Root Cause
Nonconforming Material/Component
Distribution Pattern
Nationally
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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