FDAOctober 1, 2019device
Accutorr 3 Vital Signs Monitor with NIBP valve assembly board, p/n 115-017679-00, containing software version 8.1.5 - Product Usage: The monitor is intended for spot-check monitoring physiologic parameters, including Pulse Oximetry (SpO2), Pulse Rate (PR), Non Invasive Blood Pressure (NIBP), and ...
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
NIBP valve assembly board subject to this recall includes enhancements that are not included in the current marketing clearance:1. Anti-motion feature 2. NIBP hose blockage identification function
What to do
FDA enforcement status: Terminated
Brands named
mindray ds usa inc dba mindray north americamindraymindray ds
UPCs
11501767900
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
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- CPSCLiKee Pull String Teething Toys Recalled Due to Risk of Serious Injury or Death from Choking; Violate Mandatory Standard for Toys; Sold on Amazon by ChilanTech2026-06-11
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