Model Number 101/800/080CZ |
Device Problem
Leak/Splash (1354)
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Patient Problem
No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 01/17/2022 |
Event Type
malfunction
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Manufacturer Narrative
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One unit was returned for investigation.Upon physical inspection, it was found that the complained issue could be duplicated.Dhr review was done, no issues related to the original complaint were found.
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Event Description
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It was reported that during the use of the product, leakage of air from the cuff was detected.No additional information is available for this complaint.
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Manufacturer Narrative
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One unit was returned for investigation.Upon physical inspection, it was found that the complained issue could be duplicated.Dhr review was done, no issues related to the original complaint were found.
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Event Description
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It was reported that during the use of the product, leakage of air from the cuff was detected.No additional information is available for this complaint.
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Search Alerts/Recalls
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