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HomeAPRIA HEALTHCARE LLC › Avance Flex 2.0 Negative Pressure Wound Therapy Pump

Avance Flex 2.0 Negative Pressure Wound Therapy Pump

APRIA HEALTHCARE LLC · Model APR100 · UDI-DI 00860385000855

OMP Prescription
10
510(k) clearances
9,164
Adverse events (75 deaths)
47
Recalls
100
Facilities

Description

Avance Flex Pump

Recalls

DateFirmReason
2025-01-17KCI USA, INC.Due to increase in complaints related to leak alarms
2024-11-05KCI USA, INC.Due to potential system error alarm and the inability to initiate therapy as a result of broken occlusion sensors.
2024-10-02Smith & Nephew Medical, Ltd.Due to issues with battery depletion and inability to recharge if the batteries are not appropriately maintained.
2024-03-11Smith & Nephew Medical, Ltd.Black particulate matter from the carbon filter component of the canisters entering the NPWT pump and potentially causing damage to the pump
2024-03-11Smith & Nephew Medical, Ltd.Black particulate matter from the carbon filter component of the canisters entering the NPWT pump and potentially causing damage to the pump
2020-06-08KCI USA, INC.The device may power off without notification to the user resulting in a stoppage of negative pressure wound therapy.
2020-06-04Cardinal Health 200, LLCCanisters potentially contain an oversized O-ring that cannot be installed into the mating connector on the device.
2020-06-04Cardinal Health 200, LLCCanisters potentially contain an oversized O-ring that cannot be installed into the mating connector on the device.
2019-12-02Medela IncInvia Foam Dressing Kit with FitPad could have holes in the sterile packaging.
2018-02-07Medela IncDevice may display a battery missing error.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.