MAUDE Adverse Event Report: CARDINAL HEALTH 200, LLC ARTERIOGRAM PACK (ARMMM)612; ANGIOGRAPHY/ANGIOPLASTY KIT

Model Number	SAN22ARMMN
Medical Device Problem Code	Material Separation (1562)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	06/13/2022
Type of Reportable Event	Malfunction
Event or Problem Description
Customer reported linting of the blue cotton or towels, pwtb04-stm, from the arteriogram pack, san22armmn.Fiber, wrapped around wire was very difficult to remove from the patient.There was a 10-15 delay with no injury to patient.
Additional Manufacturer Narrative
Based on investigation, the device history record review could not be verified as lot number was not provided.A sample was not returned for evaluation, therefore, a root cause could not be determined for this product.We will continue to monitor trends for this product.According to supplier, or towel is made of cotton, so cotton fiber is born.The supplier is continuously working with cardinal health to better control the linting and have implemented several measures to improve it: suctions machines have been installed in grey cloth rolling process, dyeing process, and cutting process.The suction process was added before product's final folding, and workers do it according to standard operation procedure requirement.Linting test method and acceptable criteria was stipulated to see the suction results.(=0.38g/10pieces).In the folding process, supplier used one cloth pad under 100pieces semi-finished products to avoid linting stuck onto the products during product's transfer.The complaint information was shared with the relevant sectors for their awareness.No action will be taken at this time.We will continue to monitor trends for this type of incident.

• Brand Name: ARTERIOGRAM PACK (ARMMM)612
• Common Device Name: ANGIOGRAPHY/ANGIOPLASTY KIT
• Manufacturer (Section D): CARDINAL HEALTH 200, LLC; 3651 birchwood dr.; waukegan IL 60085
• Manufacturer (Section G): MEX03 MEXICO-JUAREZ PRESOURCE; c. arcadia 1580 , col. terraza; cd.juarez , chihuahua CP 32 599; MX CP 32599
• Manufacturer Contact: patricia tucker ; 3651 birchwood dr.; waukegan, IL 60085 ; 8478874151
• MDR Report Key: 14933554
• Report Number: 1423537-2022-00801
• Device Sequence Number: 12194639
• Product Code: OEQ
• UDI-Device Identifier: 10195594554040
• UDI-Public: 10195594554040
• Combination Product (Y/N): N
• Initial Reporter State: FL
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Health Professional,User Facility
• Initial Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial
• Report Date (Section B): 07/06/2022

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: SAN22ARMMN
• Device Catalogue Number: SAN22ARMMN
• Device Lot Number: UNKNOWN
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 06/14/2022
• Initial Report FDA Received Date: 07/06/2022
• 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: Unknown
• Patient Sequence Number: 1
• Patient Sex: Female
• Patient Weight: 54 KG