MAUDE Adverse Event Report: LUMENIS LTD. SLIMLINE 200¿ REUSABLE FIBER; LASER FIBER DELIVERY DEVICE

Model Number SLIMLINE 200 REUSABLE FIBER

Device Problem Material Fragmentation (1261)

Patient Problem No Known Impact Or Consequence To Patient (2692)

Event Date 02/10/2016

Event Type  Injury  

Manufacturer Narrative

As part of a remedial activity, lumenis conducted a retrospective review of all its slimline 200 fiber complaint files from january 2015 to may 2017.An investigation of the reported event found that the reported malfunction of the slimline 200 fiber was similar to a device malfunction that was alleged to have caused or contributed to a potentially harmful situation.Because the company is aware that this malfunction was alleged to have caused or continued to a serious injury (reference mdr #3004135191-2017-00002), this event represents a reportable malfunction.The subject laser fiber was returned to the manufacturer for testing and examination.A lumenis quality engineer examined the fiber and concluded the root cause of failure to be "wear and tear - the reported device or component failure was due to long or extended use" although the doctor was able to remove the broken fiber fragment from the patient one week later and no patient harm had been reported, lumenis is also reporting this as an adverse event as medical intervention was required to preclude serious injury.

Event Description

A foreign user facility reported that a lumenis slimline 200 laser fiber broke after several minutes of use.One week later when the patient returned for another urology procedure, a two centimeter (2cm) piece of a laser fiber was found in a patient.No information regarding a report of serious injury was received.

• Brand Name: SLIMLINE 200¿ REUSABLE FIBER
• Type of Device: LASER FIBER DELIVERY DEVICE
• Manufacturer (Section D): LUMENIS LTD.; 6 hakidma street; po box 240; yokneam, 20692 ; IS 20692
• Manufacturer (Section G): LUMENIS LTD.; 6 hakidma street; po box 240; yokneam, 20692 ; IS 20692
• Manufacturer Contact: alan vaisman ; 6 hakidma street; po box 240; yokneam, 20692 ; IS 20692 ; 49599044
• MDR Report Key: 6596407
• MDR Text Key: 76129312
• Report Number: 3004135191-2017-00079
• Device Sequence Number: 1
• Product Code: GEX
• Combination Product (y/n): N
• Reporter Country Code: CA
• PMA/PMN Number: K140388
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: foreign,user facility
• Reporter Occupation: Risk Manager
• Type of Report: Initial
• Report Date: 05/29/2017

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: Yes
• Device Operator: Physician
• Device Expiration Date: 03/26/2020
• Device Model Number: SLIMLINE 200 REUSABLE FIBER
• Device Catalogue Number: 0626-221-20
• Device Lot Number: 44120415
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 06/06/2016
• Is the Reporter a Health Professional?: No
• Initial Date Manufacturer Received: 04/14/2016
• Initial Date FDA Received: 05/29/2017
• Was Device Evaluated by Manufacturer?: Yes
• Date Device Manufactured: 04/26/2015
• Is the Device Single Use?: No
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Unknown
• Patient Sequence Number: 1
• Patient Outcome(s): Required Intervention