Catalog Number 105200-000040 |
Device Problem
Deflation Problem (1149)
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Patient Problem
No Consequences Or Impact To Patient (2199)
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Event Date 04/04/2019 |
Event Type
malfunction
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Manufacturer Narrative
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(b)(4).
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Event Description
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The complaint is reported as: "when using the lma unique silicone size 4, clinicians experienced not being able to take air out of the lma through cuff pilot".The patient condition is reported as "fine".
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Event Description
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The complaint is reported as: "when using the lma unique silicone size 4, clinicians experienced not being able to take air out of the lma through cuff pilot".The patient condition is reported as "fine".
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Manufacturer Narrative
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Qn#(b)(4).Complaint verification testing could not be performed as no sample was returned for analysis.Without the device to evaluate the complaint could not be confirmed and the probable cause could not be determined from the available information.Teleflex will continue to monitor and trend for reports of this nature.
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Search Alerts/Recalls
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