PlainRecalls
FDA Devices Moderate Class II Terminated

Edwards TruWave x 2 (3 cc)/VAMP Jr/54 in (136) Kit, REF: T443952B, Pressure Monitoring Set, RX Only, CE, Sterile EO, Sterilized using ethylene Oxide, UDI: (01) 57460691930174 ***Not Marketed within the US

Reported: July 7, 2021 Initiated: May 26, 2021 #Z-1961-2021

Product Description

Edwards TruWave x 2 (3 cc)/VAMP Jr/54 in (136) Kit, REF: T443952B, Pressure Monitoring Set, RX Only, CE, Sterile EO, Sterilized using ethylene Oxide, UDI: (01) 57460691930174 ***Not Marketed within the US

Reason for Recall

There is a potential that the pressure tubing may detach from the blood sampling system

Details

Recalling Firm
Edwards Lifesciences, LLC
Units Affected
290 units
Distribution
US: AZ CA CO CT DC DE FL GA ID IL IN KY LA MA MD ME MI MN MO MS MT NC ND NE NJ PR SD TX UT VA WA WI WV OUS: Canada, United Kingdom, Italy
Location
Irvine, CA

Frequently Asked Questions

What product was recalled?
Edwards TruWave x 2 (3 cc)/VAMP Jr/54 in (136) Kit, REF: T443952B, Pressure Monitoring Set, RX Only, CE, Sterile EO, Sterilized using ethylene Oxide, UDI: (01) 57460691930174 ***Not Marketed within the US. Recalled by Edwards Lifesciences, LLC. Units affected: 290 units.
Why was this product recalled?
There is a potential that the pressure tubing may detach from the blood sampling system
Which agency issued this recall?
This recall was issued by the FDA Devices on July 7, 2021. Severity: Moderate. Recall number: Z-1961-2021.