TRUWAVE, VAMP PXVMP160Recalls & reported problems
Edwards Lifesciences LLC · PRESSURE MONITORING SET · Class 2
All models of TRUWAVE, VAMP (19)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07460691955080), received between Feb 10, 2022 and Apr 8, 2022 — classified as 2 injuries.
The most frequently reported specific device problem is “Break” (2 reports).
12 other recalls cover devices cleared under the same FDA submission (K142749, K173586, K896819); they may or may not involve this specific model.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Most reported problems
Device problems
- Break2
Patient problems
- Insufficient Information2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryApr 8, 2022Break; Break
IT WAS REPORTED AN ARTERIAL LINE TUBING OF A TRUWAVE BROKE AT THE CONNECTION. PATIENT EXPERIENCED A SERIOUS INJURY AND INTERVENTION WAS NEEDED. RECEIVED MEDWATCH REPORT. CH REACHED OUT TO CUSTOMER MULTIPLE TIMES FOR ADDITIONAL INFORMATION, BUT RECEIVED NO RESPONSE.
Patient problems: Insufficient Information
MAUDE report 14059328 ↗InjuryFeb 10, 2022Break
ARTERIAL LINE TUBING BROKE AT THE CONNECTION. FDA SAFETY REPORT ID# (B)(4).
Patient problems: Insufficient Information
MAUDE report 13514369 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K142749, K173586, K896819. One submission often covers many models, so check the product and lot details in each record.
- Z-0413-2024 · Oct 4, 2023 · Open, ClassifiedTruWave 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),
- Z-0414-2024 · Oct 4, 2023 · Open, ClassifiedTruWave with Vamp System Pressure monitoring set, REF: PXAVMP(3cc)/VAMP 68 in (173cm) PXAVMP3: x3 (3cc)/VAMP PXVK0364:(3cc)/VAMP 96in (241cm); PXVK0853: x3 (3cc)/VAMP 76in (193cm)
- Z-1963-2021 · May 26, 2021 · TerminatedEdwards VAMP Jr. 6 in (15 cm) REF: VMP306, Blood Management System, Rx Only, Single Use, CE, Sterile EO UDI: (01)57460691944782
- Z-1960-2021 · May 26, 2021 · TerminatedEdwards TruWave (30 cc)/VAMP Jr/52 in (132 cm) Kit, REF: PXVJ0711, Pressure Monitoring Set, RX Only, CE, Sterile EO, Sterilized using ethylene Oxide, UDI: (01) 07460691954489
- Z-1964-2021 · May 26, 2021 · TerminatedEdwards TruWave (30 cc)/VAMP Jr Kit, REF: VMP306PX, Pressure Monitoring Set, Rx Only, CE, UDI: (01)57460691950370
- Z-1959-2021 · May 26, 2021 · TerminatedEdwards TruWave (3 cc)/VAMP Jr 48 in (120 cm) Kit, REF: PXVJ356, Pressure Monitoring Set, RX Only, CE, Sterile EO, Sterilized using ethylene Oxide, UDI: (01) 57460691954507
- Z-1962-2021 · May 26, 2021 · TerminatedEdwards REF: VJ0990, Blood Management System, Rx Only, Single Use, CE, Sterile EO UDI: (01)57460691951520
- Z-1961-2021 · May 26, 2021 · TerminatedEdwards 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 ***N
- Z-1966-2021 · May 26, 2021 · TerminatedEdwards TruWave (3 cc)/VAMP Jr, REF: VMP406PX, Pressure Monitoring Set, Rx Only, CE UDI: (01)07460691958746
- Z-1965-2021 · May 26, 2021 · TerminatedEdwards TruWave 3 cc/VAMP Jr Kit, REF: VMP426PX, Pressure Monitoring Set, Rx Only, CE UDI: (01)57460691950547
- Z-2776-2015 · Jul 31, 2015 · TerminatedEdwards Pressure Monitoring Kit with TruWave disposable pressure transducer. A sterile, single-use kit that monitors pressures when attached to pressure monitoring catheters. For
- Z-1146-2013 · Jan 30, 2013 · TerminatedPressure Monitoring sets with VAMP Plus closed blood sampling system model # T001691A, PXVP0566, PXVP2260, PXVP0826, PXVP0827, PXVP2284AT3, PXVP23X3AT3, T398807D, T100605B, T001762
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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