MAUDE Adverse Event Report: CODMAN AND SHURTLEFF, INC ORBIT GALAXY DETACHABLE COIL SYSTEM; NEUROVASCULAR EMBOLIZATION DEVICE

Catalog Number	640CF0510
Medical Device Problem Code	Stretched (1601)
Health Effect - Clinical Code	No Consequences Or Impact To Patient (2199)
Date of Event	01/23/2017
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
This is initial/final mdr report being submitted for this complaint with associated mfr# 3008264254-2017-00029, 3008264254-2017-00027 and 3008264254-2017-00028.Additional procode: krd.(b)(4).A non-sterile orbit galaxy tdl cmplx fill coil 5x10 was received coiled inside of a coil plastic bag.The hypotube was inspected and it was found kinked at 86 and 88cm from the proximal end.The introducer was received unzipped without damage and part of the support coil was found outside of the introducer from the proximal end.The gripper and the embolic coil were found outside of the introducer.The gripper and embolic coil were inspected under microscope; the gripper was found without damage while the embolic coil was found stretched.The functional test could not be performed as part of the support coil was found outside of the introducer from the proximal end.A review of the manufacturing documentation associated with this lot 17498369 presented no issues during the manufacturing process that can be related to the reported complaint.The failure reported by the costumer as ¿delivery tube - damaged-in patient" was confirmed during the visual analysis.The kinked section found on the device was apparently caused by excessive force applied on the devices but it could not be conclusively determined.The failure reported by the customer as ¿coil ¿ impeded¿ could not be evaluated as part of the support coil was found outside of the introducer from the proximal end.Neither the dhr review nor the product analysis suggests that the failure experienced by the customer is related to the manufacturing process; handling and procedural factors could have contributed to this condition.No corrective or preventive actions will be taken.
Event or Problem Description
As reported by a health care professional, during coil embolization of an aneurysm at the internal carotid artery resistance was experienced when using two og complex fill 5x10 coils and one og xtrasoft 4x8 coil.The patient¿s vessels were not calcified.The og complex fill 5x10 coil (complaint product 1) was inserted into the micro catheter but it got stuck at the proximal portion.The physician tried to advance the coil but there was strong resistance and the delivery wire was broken.The coil was replaced with another one (complaint product2, same lot number) but the same issue occurred with it.The coil was replaced with another coil a og xtrasoft 4x8 coil (complaint 3).However it got stuck at the distal portion of the micro catheter and there was strong resistance felt.Therefore the coil was replaced with another one (competitor's product).The procedure was successfully completed without further issues or delay.There was also no patient injury / complication reported.The complaint product was new and stored per labeling instructions.The procedure was conducted in accordance with the ifu and the constant flush had been maintained at all time.No visible defect/damage was noted on the products prior to (and after) the event.No unintended detachment was observed in the vessel or in the microcatheter.The products will be returned for investigation.No further information is available.

• Brand Name: ORBIT GALAXY DETACHABLE COIL SYSTEM
• Common Device Name: NEUROVASCULAR EMBOLIZATION DEVICE
• Manufacturer (Section D): CODMAN AND SHURTLEFF, INC; 325 paramount dr; raynham MA
• MDR Report Key: 6389085
• Report Number: 3008264254-2017-00029
• Device Sequence Number: 603729
• Product Code: HCG
• UDI-Device Identifier: 10886704030294
• UDI-Public: (01)10886704030294(17)180430(10)17498369
• Combination Product (Y/N): N
• Initial Reporter Country: JA
• PMA/510(K) Number: K093973
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: company representative,foreig
• Initial Reporter Occupation: Health Professional
• Type of Report: Initial
• Report Date (Section B): 01/23/2017

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: 04/30/2018
• Device Catalogue Number: 640CF0510
• Device Lot Number: 17498369
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 02/06/2017
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 03/08/2017
• Initial Report FDA Received Date: 03/08/2017
• Patient Sequence Number: 1