MAUDE Adverse Event Report: MEX03 MEXICO-JUAREZ PRESOURCE HAND PACK (HPPSE)258; GENERAL SURGERY TRAY (KIT)

Model Number	SOP21HPPSF
Health Effect - Clinical Code	Unspecified Infection (1930)
Date of Event	12/19/2019
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
From the device history record, lot# 2508bq was manufactured on 31st aug to 06th sep 2018.No exception was recorded in the device history record that could lead to the reported incident.No sample was returned for investigation.Supplier reviewed the environment control, temperature/humidity, different pressure, air exchange time, particles, settling microbe, planktonic bacteria and surface microorganisms monitor/test record from jan 2018 to dec 2018, and all were within the specifications.There was no deviation found.According to the production environment control procedure, each workshop shall do the routine daily cleaning and comprehensive clean once or twice every week.From the investigation, the root cause could not be determined.There is no action taken at this time, but supplier will continue to monitor the trend of this type of incident.
Event or Problem Description
Customer informed cardinal health that they have noticed an increase in infections and believes it¿s in conjunction with the gown recall.This case used a cardinal health hand pack sop21hppsf that contained an aami level 3 gown 9545ncc.Gown 9545ncc was not part of the recall.The procedure was performed prior to the hold and recall notice(s) that were provided to customers beginning on 1/12/2020.Procedure performed was a left carpal tunnel release where the patient developed a surgical site infection diagnosed in a post-surgical emergency room visit.Patient is now healed.

• Brand Name: HAND PACK (HPPSE)258
• Common Device Name: GENERAL SURGERY TRAY (KIT)
• Manufacturer (Section D): MEX03 MEXICO-JUAREZ PRESOURCE; c. arcadia 1580 , col. terraza; cd.juarez , chihuahua CP 32 599; MX CP 32599
• MDR Report Key: 9741476
• Report Number: 1423537-2020-00423
• Device Sequence Number: 13903827
• Product Code: LRO
• UDI-Device Identifier: 10888439440010
• UDI-Public: 10888439440010
• Combination Product (Y/N): N
• Initial Reporter State: TN
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: health professional,user faci
• Initial Reporter Occupation: Other
• Type of Report: Initial
• Report Date (Section B): 02/21/2020

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: Yes
• Operator of Device: Health Professional
• Device Model Number: SOP21HPPSF
• Device Catalogue Number: SOP21HPPSF
• Device Lot Number: 225083
• Was Device Available for Evaluation?: Yes
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 01/22/2020
• Initial Report FDA Received Date: 02/21/2020
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Other
• Patient Age: 31 YR
• Patient Weight: 83