Outset Medical, Inc.: Device Recall

Recall #Z-2150-2024 · 04/30/2024

Class II: Risk

Recall Details

Recall Number: Z-2150-2024
Classification: Class II
Product Type: Device
Recalling Firm: Outset Medical, Inc.
Status: Ongoing
Date Initiated: 04/30/2024
Location: San Jose, CA, United States
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 431

Reason for Recall

A 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 the associated connector power entry module, which may lead to transient delay in treatment or blistering to the user.

Product Description

TabloCart with Prefiltration Drawer PN-0006813, with power cords: PN-0005746 (10-foot), PN-0006578 (15-foot), PN-0005747 (20-foot)10-, 15- and 20-foot cords respectively), used with the Tablo Hemodialysis System.

Distribution Pattern

US Nationwide distribution in the states of FL, CA, NC, GA, MD, DE, AK, OK, MA, WV, IN, KY, AZ, LA, NE, KS, NJ, CT, NM, CO, SC, TX, PA, NY, OH.

Other Recalls by Outset Medical, Inc.

Class II: Risk 08/01/2024

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.

View all recalls by Outset Medical, Inc. →

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.