Catalog Number 105200-000040 |
Device Problems
Inflation Problem (1310); Device Damaged Prior to Use (2284)
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Patient Problem
No Patient Involvement (2645)
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Event Date 01/14/2019 |
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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Customer complaint alleges "the anesthesiologists were not able to engage the one way valve to inflate/deflate the mask." no patient involvement was reported.
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Event Description
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Customer complaint alleges "the anesthesiologists were not able to engage the one way valve to inflate/deflate the mask." no patient involvement was reported.
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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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