MAUDE Adverse Event Report: ETHICON ENDO-SURGERY, LLC. ETS*ENDO ARTICU LIN CUTTER WHI; STAPLE, IMPLANTABLE

Catalog Number	ATW35
Health Effect - Clinical Code	No Consequences Or Impact To Patient (2199)
Date of Event	01/01/2017
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
(b)(4).Batch number: k5d50f.Investigation summary: the analysis showed that the ats35 device was received with no apparent damage and with a tr35w cartridge loaded in the device.The reload was received partially fired 1/4 and with the reload lockout spring damaged.The damage to the reload lockout spring is consistent with damage observed when the firing cycle is started, interrupted, released, and restarted.When firing the device make sure that the firing stroke is completed.Do not partially fire the device.Fire the device by squeezing the firing trigger completely until it rests on the closing trigger.Once the firing cycle has been initiated, it must be completed.If re-initiation of firing is resumed, the device will lock out.Firing through the lockout mechanism will break the device.Please reference the instruction for use for more information.The returned device was tested for functionality with a test reload and it fired, cut and formed all the staples as intended.The device fired without any difficulties, the staple line was complete and the staples were noted to have the proper b-formed shape.The device history records were reviewed and the manufacturing criteria were met prior to the release of this batch/lot.
Event or Problem Description
It was reported at first stapling, clamp did not function.It locked on patient but was remove without difficulties.Use of another device.No patient consequences.

• Common Device Name: STAPLE, IMPLANTABLE
• Manufacturer (Section D): ETHICON ENDO-SURGERY, LLC.; 475 calle c; guaynabo 00969
• MDR Report Key: 7156574
• Report Number: 3005075853-2018-07002
• Device Sequence Number: 13827232
• Product Code: GDW
• UDI-Device Identifier: 20705036012327
• UDI-Public: 20705036012327
• Combination Product (Y/N): N
• Initial Reporter Country: FR
• PMA/510(K) Number: K020779
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: company representative,foreig
• Initial Reporter Occupation: Other
• Type of Report: Initial
• Report Date (Section B): 12/06/2017

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: 07/24/2018
• Device Catalogue Number: ATW35
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 12/06/2017
• Initial Date Received by Manufacturer: 12/06/2017
• Initial Report FDA Received Date: 01/02/2018
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1