MAUDE Adverse Event Report: STRYKER INSTRUMENTS-PUERTO RICO INRPLS HP W/COAX MULTI-ORIFICE; LAVAGE, JET

Catalog Number	0210158000
Medical Device Problem Code	Leak/Splash (1354)
Health Effect - Clinical Code	No Consequences Or Impact To Patient (2199)
Date of Event	03/20/2019
Type of Reportable Event	Malfunction
Event or Problem Description
The user facility reported that the device leaked fluid from the battery pack during a procedure.There was no delay, no medical intervention, and no adverse consequences.
Event or Problem Description
The user facility reported that the device leaked fluid from the battery pack during a procedure.There was no delay, no medical intervention, and no adverse consequences.

• Brand Name: INRPLS HP W/COAX MULTI-ORIFICE
• Common Device Name: LAVAGE, JET
• Manufacturer (Section D): STRYKER INSTRUMENTS-PUERTO RICO; las palmas industrial park; highway #3, km 130.2; arroyo 00615
• MDR Report Key: 8496103
• Report Number: 0001811755-2019-01122
• Device Sequence Number: 1062850
• Product Code: FQH
• UDI-Device Identifier: 37613327351003
• UDI-Public: 37613327351003
• Combination Product (Y/N): N
• Initial Reporter State: NJ
• Initial Reporter Country: US
• PMA/510(K) Number: EXEMPT
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: user facility
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date (Section B): 05/13/2019

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 Catalogue Number: 0210158000
• Device Lot Number: 18276012
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 05/03/2019
• Initial Date Received by Manufacturer: 03/20/2019
• Supplement Date Received by Manufacturer: 05/10/2019
• Initial Report FDA Received Date: 04/09/2019
• Supplement Report FDA Received Date: 05/13/2019
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1