RecallRadar

FDA Device recall Z-2767-2017

DLP Pressure Monitoring Extension Line Adapters Extends the pressure line in order to reach the pressure monitoring unit during cardiopulmo…

On 2017-08-02 the FDA classified a Class II recall of DLP Pressure Monitoring Extension Line Adapters Extends the pressure line in order to reach the pressure monitoring unit during cardiopulmo… by Medtronic Perfusion Systems, citing identification of small pinholes in a single packaging configuration of sterile pouches. A total of seven different products were affected.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-2767-2017
ClassificationClass II
Statusterminated
Initiated2017-06-22
Published2017-08-02
Last updated2026-09-13 11:54 UTC
CompanyMedtronic Perfusion Systems
DistributionUS

Product

DLP Pressure Monitoring Extension Line Adapters Extends the pressure line in order to reach the pressure monitoring unit during cardiopulmonary bypass surgery.

Reason

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

Identifiers

code_info
Model No. 25009; Product UPN 20613994918608; Lot No. 2016090217, 2016091068, 2016100893, 2016110439, 2016120464, 201701…Model No. 25009; Product UPN 20613994918608; Lot No. 2016090217, 2016091068, 2016100893, 2016110439, 2016120464, 2017010278, 2017030102, 2017030576, 2017031125. Model No. 25010: Product UPN 20613994918585: Lot No. 2016020841, 2016031522, 2016050255, 2016070494, 2016081243, 2016090923, 2016110054, 2016110837, 2017040714.

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2767-2017%22

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