PlainRecalls
FDA Devices Moderate Class II Terminated

DLP Pressure Disposable Pressure Display Sets Extends the pressure line in order to reach the pressure monitoring unit during cardiopulmonary bypass surgery.

Reported: August 2, 2017 Initiated: June 22, 2017 #Z-2768-2017

Product Description

DLP Pressure Disposable Pressure Display Sets Extends the pressure line in order to reach the pressure monitoring unit during cardiopulmonary bypass surgery.

Reason for Recall

Identification of small pinholes in a single packaging configuration of sterile pouches. A total of seven different products were affected.

Details

Units Affected
63053 (48180 US) (14873 OUS)
Distribution
Worldwide Distribution - US (nationwide) Foreign: Argentina, Australia, Austria, Belgium, Bulgaria, Canada, Croatia, Denmark, El Salvador, France, Georgia, Germany, Hungary, Ireland, Israel, Italy, Japan, Kuwait, Lebanon, Macedonia, Moldova, Netherlands, New Zealand, Nigeria, Norway, Poland, Romania, Russian Federation, Slovenia, Spain, Thailand, Turkey, & United Kingdom.
Location
Brooklyn Park, MN

Frequently Asked Questions

What product was recalled?
DLP Pressure Disposable Pressure Display Sets Extends the pressure line in order to reach the pressure monitoring unit during cardiopulmonary bypass surgery.. Recalled by Medtronic Perfusion Systems. Units affected: 63053 (48180 US) (14873 OUS).
Why was this product recalled?
Identification of small pinholes in a single packaging configuration of sterile pouches. A total of seven different products were affected.
Which agency issued this recall?
This recall was issued by the FDA Devices on August 2, 2017. Severity: Moderate. Recall number: Z-2768-2017.