Outset Medical, Inc.
5 recall(s) on record — most severe on record: Class I.
Recalls by year
- Recalls (5)
Registered facilities (3)
- Baja Fur S.A. de C.V. FEI 3038138522 · MX
- Baja Fur S.A. de C.V. FEI 3017552925 · MX
- Outset Medical, Inc. FEI 3010355846 · CA
Recalls & enforcement
- Class IIOngoing2024-08-01Blood leak sensor, a component of hemodialysis device, may show decreased sensitivity, at the lowest level, specified as 0.35 mL/min blood leak rate, which could delay triggering the ALARM_DIALYZER_BLOOD_LEAK alarm, if blood loss, less-than 300ml, occurs, the patient may experien…
- Class IIOngoing2024-04-30A cart with prefiltration drawer, an optional hemodialysis system accessory, has a cord with a female connector that has internal contact pins that may become damaged that could create localized heat, sparks, smoke, melting or charring (thermal event) of the female connector or t…
- Class IOngoing2024-03-06Hemodialysis System, pre and post dialyzer peroxide-cured silicone tubing, with less than 336 hours usage, will be replaced because tubing may contain non-dioxin-like (NDL) polychlorinated biphenyl acids (PCBAs), that have not been flushed out over time with usage. Exposure to PC…
- Class IIOngoing2023-01-24An observed trend of high conductivity dialysate alarms in a hemodialysis system as a result of introducing a software tool into the manufacturing process.
- Class IIOngoing2022-01-20Due to a component in the hemodialysis console there is the possibility of heat-related damage that may occur with the device.
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. We restate the public record only — measured facts, never risk verdicts.
Cite this record
RegWarden. “Outset Medical, Inc. — FDA compliance profile.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/company/oo-10047467-outset-medical-inc/
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