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Terminated

Edwards Pressure Monitoring Kit with TruWave disposable pressure transducer. A sterile, single-use kit that monitors pressures when attached to pressure monitoring catheters. For use on patients requiring intravascular, intracranial, or intrauterine pressure monitoring.

FDA Recall Z-2776-2015 · Posted 2015-09-16

Recall StatusTerminated
Product CodeDXO
Date Initiated2015-07-31
Date Terminated2016-07-08
Product Quantity13,077 (U.S.) and 12,306 (International)

Reason for Recall

Flow restriction issues in a trifurcated IV set included in the pressure transducer kits. A restriction of the flow of IV fluid would result in either an inability to prime the system before use or difficulty in flushing the line after a blood draw.

Firm Action

Edwards sent an Urgent Product Recall Letter on August 10, 2015, to all affected customers. The letter identified the product, the problem, and the action to be taken by the customer. The firm's letter requests that customers return any of the units that they currently have in inventory. The letter requests that customers verify the inventory that has been pre-populated on the acknowledgment form, and complete the remainder of the form. The firm states to fax back the acknowledgment form within three days of receipt of notification to Edwards Customer Service at 1-800-422-9329. The firm requests to call Edwards Customer Service at 1-800-424-3278 to arrange for return of any unused product from the implicated lots as well as to obtain information about product replacment. The notification states to call for an RGA prior to returning any unused product and return unused product to the firm at Edwards Lifesciences Return Goods. Any questions the firm states to contact Edwards Customer Service at 1-800-424-3278.

Root Cause

Device Design

Distribution Pattern

Worldwide Distribution - US nationwide, Australia, Austria, Canada, China, Colombia, Croatia, Denmark, France, Germany, Great Britain, Italy, Netherlands, New Zealand, Sweden, and Slovenia.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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