MAUDE Adverse Event Report: US SURGICAL PUERTO RICO GIA PREMIUM; APPARATUS, SUTURING, STOMACH AND INTESTINAL

Model Number	030735L
Medical Device Problem Code	Failure to Fire (2610)
Health Effect - Clinical Code	No Consequences Or Impact To Patient (2199)
Date of Event	03/11/2019
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
If information is provided in the future, a supplemental report will be issued.
Event or Problem Description
According to the reporter, during an open right hemicolectomy procedure, while dividing the colon, the surgeon could not fire the device.The black pusher thumb could not be moved at all.After inspection of the reload, they noticed that there were no staples in rows.They used a new reload with the same handle, and everything gone well.There was no patient injury.

• Brand Name: GIA PREMIUM
• Common Device Name: APPARATUS, SUTURING, STOMACH AND INTESTINAL
• Manufacturer (Section D): US SURGICAL PUERTO RICO; 201 sabanetas industrial park; ponce PR 00716 4401
• MDR Report Key: 8471687
• Report Number: 2647580-2019-01759
• Device Sequence Number: 13718737
• Product Code: FHM
• UDI-Device Identifier: 10884521031630
• UDI-Public: 10884521031630
• Combination Product (Y/N): N
• Initial Reporter Country: PL
• PMA/510(K) Number: K801590
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: company representative,foreig
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial
• Report Date (Section B): 04/01/2019

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 Expiration Date: 07/31/2023
• Device Model Number: 030735L
• Device Catalogue Number: 030735L
• Device Lot Number: P8G1401X
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 03/11/2019
• Initial Report FDA Received Date: 04/01/2019
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1