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Terminated

Pulsiocath PiCCO ProAQT Monitoring Kit, single-use cardiac output (CO) sensor, one unit per plastic sterilizable package. Product Usage: Measures cardiac output by the thermodilution method, measurement of arterial blood pressure, and for cardiac output determination by arterial pulse contour analysis.

FDA Recall Z-1121-2015 · Posted 2015-02-17

Recalling FirmPulsion Medical Inc
Recall StatusTerminated
Product CodeKRB
Date Initiated2014-11-04
Date Terminated2015-10-02
Product Quantity90 units

Reason for Recall

Internal testing and investigation of the packaging revealed cracks and holes in primary packaging

Firm Action

Pulsion sent an Urgent Medical Device Recall notification letter on 11/04/14 to affected customers. The letter identified the affected product, problem and actions to be taken. Customers where instructed to: " Piease examine your inventory immediately to determine if you have any of the products listed. " lf so, please remove the affected products; quarantine them in a secure location. " Piease complete and return the enclosed Field Recall Response Form, acknowleding your receipt and understanding of this communication " Send all affected products back to PULSION Medical Systems. " Upon return of the affected product you will receive a credit note. For questions contact your PULSION Medical lnc Recall Coordinator.

Root Cause

Packaging

Distribution Pattern

US Nationwide Distribution in the states of CT, NJ and NY. The affected product was distributed to one government consignee.

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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