Catalog Number SAC-00818-PBX |
Device Problems
Incorrect, Inadequate or Imprecise Result or Readings (1535); Obstruction of Flow (2423)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 01/30/2023 |
Event Type
malfunction
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Event Description
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It was reported that: the arterial catheter was inserted in the right radial on (b)(6) at 11 p.M and on the (b)(6) at 2 p.M.It was not functional anymore.The arterial pressure was impossible to get, sample impossible.Another device was inserted.The patient's current condition was reported as "out of the department".
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Manufacturer Narrative
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Qn#(b)(4).
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Manufacturer Narrative
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(b)(4).Complaint verification testing could not be performed as it was reported that the sample is not available for return.A device history record review was performed and no relevant findings were identified.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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Event Description
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It was reported that: the arterial catheter was inserted in the right radial on 29 january at 11 p.M and on the 31 january at 2 p.M.It was not functional anymore.The arterial pressure was impossible to get, sample impossible.Another device was inserted.The patient's current condition was reported as "out of the department".
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Search Alerts/Recalls
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