MAUDE Adverse Event Report: STRYKER ENDOSCOPY-SAN JOSE PKG., 4MM AUTOCLAVABLE ARTHROSCOPE

Model Number	0502477031
Medical Device Problem Codes	Poor Quality Image (1408); Nonstandard Device (1420)
Health Effect - Clinical Codes	Insufficient Information (4580); No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	08/05/2020
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
Additional information will be provided once the investigation has been completed.The device manufacturer date is not known at this time.However, should it become available it will be provided in future reports.
Event or Problem Description
It was reported that there was a poor image.
Additional Manufacturer Narrative
The device was not received for investigation at stryker endoscopy because it was repaired locally in poland.The technical service report is attached, and indicates: broken inner lens, hazy.Probable root cause: poor mate between cannula and endoscope; poor fit between endoscope needle and cannula; use error.The reported failure mode will be monitored for future reoccurrence.Manufacture date is not known.
Event or Problem Description
It was reported that there was a poor image.

• Brand Name: PKG., 4MM AUTOCLAVABLE ARTHROSCOPE
• Common Device Name: ARTHROSCOPE
• Manufacturer (Section D): STRYKER ENDOSCOPY-SAN JOSE; 5900 optical court; san jose CA 95138
• MDR Report Key: 10501954
• Report Number: 0002936485-2020-00365
• Device Sequence Number: 304642
• Product Code: HRX
• UDI-Device Identifier: 07613327059137
• UDI-Public: 07613327059137
• Combination Product (Y/N): N
• Initial Reporter Country: PL
• PMA/510(K) Number: K962075
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: other
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date (Section B): 10/15/2020

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 Model Number: 0502477031
• Device Catalogue Number: 0502477031
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 08/11/2020
• Initial Date Received by Manufacturer: 08/11/2020
• Supplement Date Received by Manufacturer: 08/11/2020
• Initial Report FDA Received Date: 09/08/2020
• Supplement Report FDA Received Date: 10/16/2020
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1