MAUDE Adverse Event Report: O&M HALYARD, INC. XTRA TRACTION SHOECOVER; PROTECTIVE APPAREL

Model Number	69252
Medical Device Problem Code	Device Unsafe to Use in Environment (2918)
Health Effect - Clinical Code	Fall (1848)
Date of Event	01/09/2025
Type of Reportable Event	Malfunction
Event or Problem Description
Incident one: (b)(6) hospital has had several falls in their l&d area.Customer suspects it could have something to do with residual powder or something coming off the shoe covers.Additional information was requested on (b)(6) 2025, with no response received back from the customer.Based on complaint report with minimal information, at this time it's unknown if there were any serious injuries or medical intervention required due to reported falls.The customer also did not provide a lot number.
Additional Manufacturer Narrative
Incident one of two: the product involved in the event is not available for return.O&m halyard, inc.Is the specification developer and complaint handling establishment of the halyard* x-tra traction* shoe cover blue univ.The complaint component halyard* x-tra traction* shoe cover blue univ, part number 69252 is contract manufactured by (b)(6) (fda registration number (b)(4)).Supplier corrective action request (scar) was submitted to the manufacturer on (b)(6) 2025.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 21cfr803, in compliance with the medical device reporting requirement and should not be considered to be an admission that an o&m halyard, inc.Product is defective or has caused serious injury.
Additional Manufacturer Narrative
Incident one of two.No samples were available for evaluation.A device history record evaluation was unable to be performed as a lot number was not provided by the customer.There have been no changes to the glue supplier.The manufacturer reviewed all outgoing inspection records of this product 69252 from jan 2024 to jan 2025, and found no problems similar to the complaint.The approximate production quantity during this period is (b)(4) cases.A wear test for 15 minutes is conducted for each lot manufactured.Some retained samples of various lots were evaluated.There were no abnormalities detected.A wear test was conducted in office, production and laboratory environments, there were no reported instances of slippage.Glue coating was acceptable post test.The manufacturer has implemented additional testing in the cutting work shop.The manufacturer has increased the amount of glue applied on the fabric.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 21cfr803, in compliance with the medical device reporting requirement and should not be considered to be an admission that an o&m halyard, inc.Product is defective or has caused serious injury.

• Brand Name: XTRA TRACTION SHOECOVER
• Common Device Name: PROTECTIVE APPAREL
• Manufacturer (Section D): O&M HALYARD, INC.; 1220 old alpharetta rd; ste 320; alpharetta GA 30005
• Manufacturer (Section G): HUBEI XINXIN NON-WOVEN CO., LTD; taizihu industrial park; pengchang town xiantao; hubei, china 43301 8; CH 433018
• Manufacturer Contact: nichole coggins ; 1220 old alpharetta rd; ste 320; alpharetta, GA 30005 ; 8287820529
• MDR Report Key: 21235931
• Report Number: 3014421917-2025-00005
• Device Sequence Number: 8075522
• Product Code: FXP
• UDI-Device Identifier: 30680651692529
• UDI-Public: 30680651692529
• Combination Product (Y/N): N
• Initial Reporter State: WA
• Initial Reporter Country: US
• PMA/510(K) Number: EXEMPT
• 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): 03/19/2025

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: 69252
• Device Catalogue Number: 69252
• Device Lot Number: UNKNOWN
• 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: 01/09/2025
• Supplement Date Received by Manufacturer: 03/12/2025
• Initial Report FDA Received Date: 01/24/2025
• Supplement Report FDA Received Date: 03/19/2025
• Was Device Evaluated by Manufacturer? (Y/N): No
• 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