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RHYTHM HEALTHCARE

Rhythm Healthcare, LLC · Model LM5BA · UDI-DI 06978651650070

CAW Prescription
1
510(k) clearances
52,921
Adverse events (527 deaths)
44
Recalls
87
Facilities

Description

The Oxygen Concentrator is a PSA oxygen generator. The PSA (pressure swing adsorption) oxygen generator is an air separation unit which is based on molecular sieves selective adsorption of nitrogen from air. It can continuously generate oxygen with the purity 93%±3% at ambient temperature. The adsorbed nitrogen can be desorbed by decreasing the adsorbed bed pressure resulting cyclical adsorption-desorption operation. The Oxygen Concentrator provides supplemental low flow oxygen therapy for adult in the home, nursing homes, patient care facilities, etc. It is available by prescription only under the supervision of a physician, and it’s not intended to support or sustain life.

Recalls

DateFirmReason
2026-02-043B Medical, Inc.Devices which did not meet internal quality specifications were inadvertently distributed.
2025-10-07Philips Respironics, Inc.Certain serial numbers of the SimplyGo Mini standard battery kit contain a defective chip which can lead the battery to either fail to charge or lose voltage output when in use in
2025-05-08Ohio Medical CorporationErroneous calibration values, potentially resulting in: as the device ages, oxygen purity will gradually decrease to the point where the device alarms to indicate low oxygen purit
2025-04-11Medical Depot Inc.Potential for DC Power Supply housing to become hot to the touch and deform the plastic housing.
2024-12-09JIANGSU JUMAO X-CARE MEDICAL EQUIPMENT CO LTDOxygen concentrator may melt or catch on fire during use.
2024-10-04Caire, Inc.Potential failure of affected units to recharge the battery of the oxygen concentrators.
2024-10-04Caire, Inc.Potential failure of affected units to recharge the battery of the oxygen concentrators.
2024-10-04Caire, Inc.Potential failure of affected units to recharge the battery of the oxygen concentrators.
2024-10-04Caire, Inc.Potential failure of affected units to recharge the battery of the oxygen concentrators.
2023-03-09DeVilbiss Healthcare LLCThe instruction manual is being replaced with an updated version that is in alignment with labeling requirements specified in the IEC-60101-1 standard.

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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.