| Catalog Number |
M8726 |
| Medical Device Problem Code |
Material Separation (1562)
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| Health Effect - Clinical Code |
No Consequences Or Impact To Patient (2199)
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| Date of Event |
01/01/2019
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Type of Reportable Event
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Malfunction
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Additional Manufacturer Narrative
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(b)(4).Attempts have been made to retrieve the device.To date the device has not been returned.If the device or further details are received at a later date a supplemental medwatch will be sent.The single complaint was reported with multiple events.There are no additional details regarding additional patient events.Attempts were made to obtain the following information.If further details are received at a later date a supplemental medwatch will be sent.Specific number of procedure involved.For each procedure please provide following separately: event date.Quantity involved.When did each involved device had the needle pulled off? lot involved.The following information was obtained: i was unable to get specific data on cases and dates as this happened over a several week period.Cases were cv and vascular.I was told that the needles were falling off right from the start or very early in the case.Note: events have been reported via mw 2210968-2019-82830, 2210968-2019-82831, 2210968-2019-82832, 2210968-2019-82834, 2210968-2019-82837.
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Event or Problem Description
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It was reported that the patient underwent a vascular or heart procedure on unknown date and suture was used.During the procedure, the needle is popping off very fast.The procedure was completed with another device of the same product code and different lots.There were no patient consequences reported.
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Additional Manufacturer Narrative
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(b)(4).Device evaluation summary: seven representative samples of product code m8726, lot # mhh994 were returned for evaluation.The complaint sample was not received.The product code is multistrand count and each packet contains four strands double armed.During the visual inspection of seven samples, no defects were found on the packages.The samples were opened, and the swage and attachment area were noted to be as expected.The sutures were dispensed without problems and examined along of the strand and no defects, or damaged were observed.A functional test was performed and the pull force were above the minimum requirements.Per the conditions of the samples received, no performance pull off suture needle was found, and the tested samples met the finished goods requirements.A manufacturing record evaluation was performed for the finished device lot number mhh994, and no non-conformances related to the reported complaint condition were identified.
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Search Alerts/Recalls
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