MAUDE Adverse Event Report: O&M HALYARD, INC. HALYARD* POLYISOPRENE MICRO POWDER-FREE STERILE SURGICAL GLOVES - 8.0; SURGICAL GLOVES POLYISOPRENE

Model Number	48320
Medical Device Problem Code	Material Puncture/Hole (1504)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	06/28/2023
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
The product involved in the event was not available for return.The complaint component surgical polyisoprene gloves, part number 48320 is manufactured by ansell (fda registration 8041180).A supplier corrective action (scar) was submitted to the manufacturer on (b)(6) 2023.A follow-up report will be provided upon conclusion of investigation and response by the manufacturer.This product incident is documented in the o&m halyard, inc.Complaint database and identified as complaint (b)(4).This information is submitted pursuant to (b)(4), in compliance with the medical device reporting requirement and should not be considered to be an admission that a o&m halyard, inc.Product is defective or has caused serious injury.
Event or Problem Description
An incident occurred using the gloves during use with a patient.There was no medical intervention/injury that occurred on the part of the user or the patient.This incident caused a breach in sterility.Provided the hole was discovered during procedure, the site has evaluated that this incident could cause a serious injury or illness should it recur during a surgical procedure and is therefore being reported as a malfunction.
Additional Manufacturer Narrative
The product involved in the event was not available for return.The complaint product was manufactured by ansell (fda registration: 8041180).O&m halyard, inc.Submitted initial mdr in error.O&m halyard, inc.Is the initial importer of device; however, there was no serious injury or illness (adverse event) associated with this complaint therefore pursuant to 21 cfr 803 a report to fda is not required by the initial importer.The manufacturer did respond to supplier corrective action request with investigation findings.No samples were provided by the customer.The retained samples were reviewed.No abnormalities were found.The device history record was reviewed, no issues were found.The product inspections were conforming with no noted issues.There was no stock of the finished good available at time of investigation.The manufacturer was unable to define a root cause.They did perform a validation in (b)(6) 2023 to improve the homogeneity of the coagulant application.The manufacturing site will continue to monitor the defects per million for period (b)(6) 2023 to ensure no complaint trends are noted subsequent to this process improvement.This product incident is documented in the o&m halyard, inc.Complaint database and identified as complaint (b)(4).

• Common Device Name: SURGICAL GLOVES POLYISOPRENE
• Manufacturer (Section D): O&M HALYARD, INC.; 1 edison drive; alpharetta GA 30005
• Manufacturer (Section G): ANSELL LANKA (PVT.), LTD.; biyagama export processing zon; biyagama gampaha,, sri lanka ; CE
• Manufacturer Contact: nichole early ; 1 edison drive; alpharetta, GA 30005 ; 8287820529
• MDR Report Key: 17419218
• Report Number: 3014421917-2023-00006
• Device Sequence Number: 8975402
• Product Code: KGO
• UDI-Device Identifier: 30680651483202
• UDI-Public: 30680651483202
• Combination Product (Y/N): N
• Initial Reporter State: WV
• Initial Reporter Country: US
• PMA/510(K) Number: K071746
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Health Professional,User Facility
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 10/17/2023

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: 48320
• Device Catalogue Number: 104832000
• Device Lot Number: 2207045005
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Was the Report Sent to FDA?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 06/28/2023
• Supplement Date Received by Manufacturer: 09/22/2023
• Initial Report FDA Received Date: 07/28/2023
• Supplement Report FDA Received Date: 10/17/2023
• Was Device Evaluated by Manufacturer? (Y/N): Device Not Returned to Manufacturer
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Patient Sex: Unknown