MAUDE Adverse Event Report: MEDOS INTERNATIONAL SARL MICRUSFRAME14 5MM X 12CM; NEUROVASCULAR EMBOLIZATION DEVICE

Catalog Number	MFR140512
Medical Device Problem Code	Stretched (1601)
Health Effect - Clinical Code	No Consequences Or Impact To Patient (2199)
Date of Event	02/25/2019
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
(b)(4).Information regarding patient identifier, date of birth, age, gender, weight, race, ethnicity, and medical history were not provided.Procode is krd/hcg.Physical manufacturer name: codman and shurtleff inc., dba depuy synthes products, inc.((b)(4)).The healthcare professional reported that during the coil embolization procedure, the 5mm x 12cm micrusframe 14 coil (mfr140512 / s14765) is one of three coils that were reported as not being able to advance through the hub of the sl-10® microcatheter (stryker).The micrusframe coil was removed and there was no observed damage on the coil.It was confirmed that adequate and continuous flush was maintained through the microcatheter.There was no kink or bend on the coil; the microcatheter was also not kinked nor have any bend on it; the same microcatheter was used to complete the procedure using competitor¿s coils.There was no report of loss of cerebral target position.There was no report of patient adverse event or significant procedural delay associated with the reported event.The 5mm x 12cm micrusframe 14 coil was returned for evaluation.The investigational finding is documented below.Investigation summary: the non-sterile 5mm x 12cm micrusframe 14 coil was returned with the other concomitant products used during the procedure.The sl-10® microcatheter (stryker) was also received.It was noted that the microcatheter was still attached to a y-connector and there was no damage noted on the microcatheter.The returned device underwent visual inspection.There was no damage observed on the hub and the device positioning unit (dpu).The marker band was observed at 47.3 cm from the hub; this is within specification.The coil introducer was unzipped and kinked.The resheathing tool was without damage.The embolic coil was detached, tangled with the device and in stretched condition.Microscopic inspection was performed on the device.The v-notch was in good condition, the resistance heating (rh) was also in good condition and showed no evidence of being heated.The embolic coil was confirmed to be stretched.The device could not undergo functional testing due the condition of the coil introducer being kinked and unzipped.The reported issue documented in the complaint that the 5mm x 12cm micrusframe 14 coil could not be advanced through the hub of the sl-10® microcatheter could not be confirmed through functional analysis as the returned device could not undergo functional testing due to the kinked and unzipped coil introducer.A review of manufacturing documentation associated with this lot (s14765) presented no issues during the manufacturing or inspection processes related to the reported complaint.There were no nonconformances related to device manufacture or inspection.All product rejected during manufacturing was identified as scrap and properly accounted for.Coil stretching is a known potential issue associated with the use of this device.The ifu provides proper handling instructions for the device to prevent such issue from occurring.Stretching can occur during attempts to withdrawal the coil against resistance.The complaint reported that the coil could not advance through the hub of the microcatheter; it is possible that in the attempt to withdraw the coil, the coil became stretched.The exact cause of the stretched condition of the coil was not conclusively determined.Based on the device history record review, there is no indication that the event is related to the device manufacturing process.In addition, devices undergo 100% inspection at final assembly for the condition of the embolic coil.Thus, it is not likely that the 5mm x 12cm micrusframe 14 coil left the manufacturing facility with the embolic coil in a stretched condition.As part of the post market surveillance program, information from this complaint is trended for statistical signals and corrective/preventive action may be triggered at a later time.Since there was no evidence to suggest the event was related to a manufacturing or design issue, no corrective actions will be taken at this time.This is one of 2 products involved with the reported complaint.The associated manufacturer report numbers are: 3008114965-2019-01007 and 3008114965-2019-01008.The manufacturer will submit a supplemental report if new facts arise which materially alter information submitted in a previous mdr report.Additional information will be submitted within 30 days of receipt.
Event or Problem Description
The healthcare professional reported that during the coil embolization procedure, the 5mm x 12cm micrusframe 14 coil (mfr140512 / s14765) is one of three coils that were reported as not being able to advance through the hub of the sl-10® microcatheter (stryker).The micrusframe coil was removed and there was no observed damage on the coil.It was confirmed that adequate and continuous flush was maintained through the microcatheter.There was no kink or bend on the coil; the microcatheter was also not kinked nor have any bend on it; the same microcatheter was used to complete the procedure using competitor¿s coils.There was no report of loss of cerebral target position.There was no report of patient adverse event or significant procedural delay associated with the reported event.The products were returned for evaluation which revealed that the 5mm x 12cm micrusframe 14 coil was in a stretched condition.Based on the product analysis completed on 4/23/2019, this event has been deemed mdr reportable as a ¿malfunction.¿.

• Brand Name: MICRUSFRAME14 5MM X 12CM
• Common Device Name: NEUROVASCULAR EMBOLIZATION DEVICE
• Manufacturer (Section D): MEDOS INTERNATIONAL SARL; chemin-blanc 38; le locle neuchatel CH-24 00; SZ CH-2400
• MDR Report Key: 8552828
• Report Number: 3008114965-2019-01007
• Device Sequence Number: 10855975
• Product Code: KRD
• UDI-Device Identifier: 10886704077992
• UDI-Public: 10886704077992
• Combination Product (Y/N): N
• Initial Reporter State: GA
• Initial Reporter Country: US
• PMA/510(K) Number: K150319
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: company representative,health
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial
• Report Date (Section B): 02/25/2019

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: Health Professional
• Device Expiration Date: 07/31/2020
• Device Catalogue Number: MFR140512
• Device Lot Number: S14765
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 04/09/2019
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 04/23/2019
• Initial Report FDA Received Date: 04/25/2019
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1