MAUDE Adverse Event Report: MEX03 MEXICO-JUAREZ PRESOURCE CATH PACK (CPBSC)885; GENERAL SURGERY TRAY (KIT)

Model Number	SAN37CPBSD
Health Effect - Clinical Code	No Known Impact Or Consequence To Patient (2692)
Date of Event	01/01/1980
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
Based on supplier investigation, the device history record could not be reviewed, as the lot number was not provided.At the time of this investigation the samples had not been received for evaluation.The linting test data was within the acceptable range, and there was no abnormal situation reported during production, therefore, the root cause could not be determined from this investigation.The complaint information was informed to the relevant sectors for their awareness.There is no action taken at this time, however, the supplier will continue to monitor the trend of this type of incident.According to our supplier, or towels are made of cotton, so lint is born and inevitable.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/10 pieces).In the folding process, the supplier used one cloth pad under 100 pieces semi-finished products to avoid linting stuck onto the products during product's transfer.
Event or Problem Description
Based on information from customer, they are still reportedly experiencing linting of towels in their custom pack.No further information could be obtained from the customer.
Additional Manufacturer Narrative
Based on supplier investigation, the device history record could not be reviewed, as the lot number was not provided.Thirteen pieces of samples were returned for investigation.No obvious abnormal situation was found on the towels.The linting test data is 0.249g / 13 pieces.The linting test data was within the acceptable range, therefore the root cause could not be determined from this investigation.Per our supplier, or towels are made of cotton, so lint is born and inevitable.We are continuously working to better control the linting and have implemented the following: 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/10 pieces).In the folding process, the supplier used one cloth pad under 100 pieces semi-finished products to avoid linting stuck onto the products during product's transfer.

• Brand Name: CATH PACK (CPBSC)885
• 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: 9233321
• Report Number: 1423537-2019-00364
• Device Sequence Number: 16916824
• Product Code: LRO
• UDI-Device Identifier: 10888439054286
• UDI-Public: 10888439054286
• Combination Product (Y/N): N
• Initial Reporter State: TX
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: user facility
• Initial Reporter Occupation: Other
• Remedial Action: Other
• Type of Report: Initial,Followup
• Report Date (Section B): 12/05/2019

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: SAN37CPBSD
• Device Catalogue Number: SAN37CPBSD
• Device Lot Number: UNKNOWN
• Was Device Available for Evaluation?: No
• Initial Date Received by Manufacturer: 10/03/2019
• Supplement Date Received by Manufacturer: 10/03/2019
• Initial Report FDA Received Date: 10/24/2019
• Supplement Report FDA Received Date: 12/05/2019
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Other