MAUDE Adverse Event Report: COVIDIEN LP LLC NORTH HAVEN Signia; STAPLE, IMPLANTABLE

Model Number SIGPHANDLE

Device Problems Entrapment of Device (1212); Unintended Head Motion (1284); Difficult to Open or Close (2921); Unintended Movement (3026)

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

Event Date 09/05/2017

Event Type  malfunction  

Manufacturer Narrative

A good faith effort will be made to obtain the applicable information relevant to the report.If information is provided in the future, a supplemental report will be issued.

Event Description

According to the reporter, while transecting the stomach on a laparoscopic roux-en-y gastric bypass on (b)(6) 2017, the instrument began to angulate after introducing into the abdominal cavity and not using the functional button.When the surgeon wanted to do an action, the device did not do command such as open, close, angulate and rotate.After opening the loading unit, the blue button was pulled back to unlock the loading unit.In this moment the device begins to rotate and angulate.Second reload's jaws was also locked on the tissue and wait some seconds and press the button again to open it.They changed the instrument and the power shell to resolve the issue in order to complete the case.There was no patient injury.

• Brand Name: Signia
• Type of Device: STAPLE, IMPLANTABLE
• Manufacturer (Section D): COVIDIEN LP LLC NORTH HAVEN; 195 mcdermott rd; north haven 06473
• Manufacturer (Section G): COVIDIEN LP LLC NORTH HAVEN; 195 mcdermott rd; north haven 06473
• Manufacturer Contact: sharon murphy ; 60 middletown ave; north haven, CT 06473 ; 2034925267
• MDR Report Key: 6894952
• MDR Text Key: 87395122
• Report Number: 1219930-2017-07430
• Device Sequence Number: 1
• Product Code: GDW
• UDI-Device Identifier: 10884521543782
• UDI-Public: 10884521543782
• Combination Product (y/n): N
• Reporter Country Code: GM
• PMA/PMN Number: K160176
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: foreign,health professional,u
• Reporter Occupation: Health Professional
• Type of Report: Initial
• Report Date: 09/05/2017

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 09/26/2017
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Operator: Health Professional
• Device Model Number: SIGPHANDLE
• Device Catalogue Number: SIGPHANDLE
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Date Manufacturer Received: 09/05/2017
• Is the Device Single Use?: No
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: N
• Patient Sequence Number: 1
• Patient Weight: 157