MAUDE Adverse Event Report: OLYMPUS MEDICAL SYSTEMS CORP. SINGLE USE REPOSITIONABLE CLIP; SINGLE USE REPOSITIONAL CLIP

Model Number	HX-202UR
Medical Device Problem Code	Device Fell (4014)
Health Effect - Clinical Code	No Known Impact Or Consequence To Patient (2692)
Date of Event	10/16/2019
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
Device was returned for evaluation.The returned hx-202ur quick clip (lot 96k 26) was evaluated due to "device failed" issue.The reported complaint is confirmed.Visual inspection was performed on the received condition.The device was determined that it has been deployed.Further evaluation determined that the clip was broken, spring was visible and the clip pipe was missing.The missing clip pipe was not included with the returned device.The insertion portion was checked and did not find any external damages.The slider was manipulated and the movement is consistent and smooth.The yellow tube joint was observed and found no damages.In summary, based on the evaluation, the reported issue was confirmed however, the exact root cause of the broken clip was not able to determine.
Event or Problem Description
It was reported that during an unspecified procedure, customer had an issue with the clip.The clip fell into the patient.The procedure was prolonged due to the issue, however, there was no patient harm or injury reported due to the event.

• Brand Name: SINGLE USE REPOSITIONABLE CLIP
• Common Device Name: SINGLE USE REPOSITIONAL CLIP
• Manufacturer (Section D): OLYMPUS MEDICAL SYSTEMS CORP.; 2951 ishikawa-cho; hachioji-shi, tokyo-to 192-8 507; JA 192-8507
• MDR Report Key: 9312415
• Report Number: 8010047-2019-03942
• Device Sequence Number: 11295681
• Product Code: PKL
• UDI-Device Identifier: 04953170385933
• UDI-Public: 04953170385933
• Combination Product (Y/N): N
• Initial Reporter State: NY
• Initial Reporter Country: US
• PMA/510(K) Number: K123601
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: company representative,user f
• Initial Reporter Occupation: Other
• Type of Report: Initial
• Report Date (Section B): 11/12/2019

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 Model Number: HX-202UR
• Device Lot Number: 96K
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 11/06/2019
• Was the Report Sent to FDA?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 10/16/2019
• Initial Report FDA Received Date: 11/12/2019
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1