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 04/17/2019 |
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: the customer is unable to deflate the cuff properly.There was no report of patient injury.
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Event Description
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The complaint is reported as: the customer is unable to deflate the cuff properly.There was no report of patient injury.
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Manufacturer Narrative
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(b)(4).Complaint verification testing could not be performed as no sample was returned for analysis.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.If the sample becomes available at a later date a follow up report will be submitted with investigation results.
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Search Alerts/Recalls
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