ClearanceBrief
Recall Z-0413-2024 ยท DRS Transducer, Blood-Pressure, Extravascular

Edwards Lifesciences, LLC

TruWave Pressure monitoring set, REF: PX212: cc/12 in (30cm), PX260: (3 cc/60in (150cm), PX272: 3 cc/72in (180cm), PX284: 3 cc/84 in (210 cm), PX2X2: x2 (3cc), PX3X3284C: X3 (3cc), PX4X4: x4 (3cc), PX600F (3cc), PXMK1876: x 3 (3 cc), PXMK1940: (3 cc), PXMK2024: (3cc)/77 in (196cm),PXMK2041: (3 cc), PXMK2321: (3cc)/48in (122cm), PXMK2331: x4 (3cc)/12 in (30cm), PXMK9146: x 2 (3cc), PXMK1876: x3(3cc

DateNov 29, 2023 (initiated Oct 4, 2023)
StatusOpen, Classified
ReasonTheir is the potential for flushing difficulties during setup of the pressure monitoring kit with pressure transducer.
Root causeDevice Design
ActionOn 10/18/2023, Edwards Lifesciences issued a "Urgent: Medical device Correction Action via FedEx mail. Edwards ask consignees to take the following actions: 1. Follow the IFU for proper setup and flushing of your device. 2. Follow the instructions included in the enclosed customer acknowledgement form to complete the acknowledgement process. 3. Verify your inventory on the attached customer acknowledgement form. 3a.E-mail the completed form to Edwards Customer Service at US.FCA@edwards.com, within 15 days from receipt of this notification. 4. Distribute this notice within your organization
Quantity118,570 units
DistributionUS: AK AL AR AZ CA CO CT DC DE FL GA HI IA ID IL IN KS KY LA MA MD ME MI MN MO MS MT NC ND NE NH NJ NM NV NY OH OK OR PA PR RI SC SD TN TX UT VA WA WI WV WY OUS: Argentina Australia Austria Bahrain Belgium Brazil Canada CANARY ISLANDS Chile Colombia Costa Rica Czech Republic Denmark Ecuador Faroe I
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K142749TruWave Disposable Pressure Transducer
Edwards Lifesciences, LLC, Jan 18, 2015
K171996TruWave Disposable Pressure Transducer
Edwards Lifesciences, LLC, Oct 23, 2017
K183413TruWave Disposable Pressure Transducer
Edwards Lifeciences, LLC, May 1, 2019