FDAAugust 1, 2024device

Tablo Console, REF: PN-0003000, PN-0006000, part of the Tablo Hemodialysis System. The Tablo Hemodialysis System is indicated for use in patients with acute and/or chronic renal failure, with or without ultrafiltration, in an acute or chronic care facility.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Blood 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 experience hypotension, fatigue, cramps, dizziness, headaches, nausea, and shortness of breath.

What to do

FDA enforcement status: Ongoing

Brands named

outset medicaloutset

UPCs

0085000101111200850001011204

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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