FDA Says Smiths Medical Issues Correction For ParaPAC Plus P300 And P310 Ventilators Due To Inadvertent Tidal Volume Knob Movement; Recall Involves Correcting Devices Without Removing Them From Use Or Sale
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Smiths Medical has issued a correction for its ParaPAC Plus P300 and P310 ventilators due to an issue with the tidal volume knob, as reported by the FDA. The recall involves correcting the devices without removing them from use or sale.
September 30, 2024 | 6:24 pm
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Smiths Medical, a subsidiary of ICU Medical (ICUI), is correcting its ParaPAC Plus P300 and P310 ventilators due to a tidal volume knob issue. The FDA reports that the recall involves fixing the devices without removing them from use or sale.
The correction of the ventilators by Smiths Medical, a part of ICU Medical, addresses a specific issue without removing the devices from the market. This suggests a limited operational impact, likely resulting in a neutral short-term effect on ICUI's stock price.
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