Model Number 0684-00-0470-01 |
Device Problem
Difficult to Remove (1528)
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Patient Problems
No Consequences Or Impact To Patient (2199); No Clinical Signs, Symptoms or Conditions (4582)
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Event Date 12/13/2020 |
Event Type
malfunction
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Manufacturer Narrative
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The device has not been returned to the manufacturer so we are unable to complete an evaluation.If provided we will send a supplemental report with our additional findings.Complaint record id #(b)(4).
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Event Description
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It was reported that the intra-aortic balloon (iab) was inserted on a patient post ablation and code.After approximately two days, the customer attempted to removed the iab but was unable to.The iab was successfully removed in the operating room.There was no patient harm or adverse event reported.
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Manufacturer Narrative
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The device has not been returned to the manufacturer so we are unable to complete an evaluation.If provided we will send a supplemental report with our additional findings.Reference complaint # (b)(4).
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Event Description
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It was reported that the intra-aortic balloon (iab) was inserted on a patient post ablation and code.After approximately two days, the customer attempted to removed the iab but was unable to.The iab was successfully removed in the operating room.There was no patient harm or adverse event reported.
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Event Description
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It was reported that the intra-aortic balloon (iab) was inserted on a patient post ablation and code.After approximately two days, the customer attempted to removed the iab but was unable to.The iab was successfully removed in the operating room.There was no patient harm or adverse event reported.
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Manufacturer Narrative
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The device has not been returned to the manufacturer so we are unable to complete an evaluation.If provided we will send a supplemental report with our additional findings.The failure mode is addressed in the risk file and is operating within its risk profile.The ifu addresses the reported failure.There were no ncmrs identified which could cause or contribute to the reported failure.The investigation does not indicate that the device was inadvertently released as non-conforming or an adulterated product or was a counterfeit.The complaint history review did not identify an adverse trend (increase in number of complaints over past three (3) months).Based on the rational provided above, no escalation to the capa process is required.Reference complaint #(b)(4).
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Search Alerts/Recalls
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