MAUDE Adverse Event Report: APPLIED MEDICAL RESOURCES CFF75, 12X75 KII FIOS ADVFIX 6/BX; LAPAROSCOPE, GENERAL & PLASTIC SURGERY

Model Number	CFF75
Medical Device Problem Code	Device Contaminated During Manufacture or Shipping (2969)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	08/11/2021
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
The event unit returned to applied medical for evaluation.A follow-up report will be provided upon completion of the investigation.
Event or Problem Description
Name of procedure being performed: na.Incoming inspection detailed description of event: [name] incoming inspection po# (b)(4).This is a complaint from [name] evaluation team.The lot mentioned above was found to have defective units per our incoming inspection.Delivery date: (b)(6) 2021.Photos are available.Products available for return.Hairlike object in pouch: cff75 lot # 1420215 (1 ea).Patient status: na (no patient involvement) type of intervention: na incoming inspection.
Additional Manufacturer Narrative
The event unit was returned to applied medical for evaluation.Visual inspection confirmed the presence of hair inside the sterile unopened pouch.Based on the condition of the returned unit and the description of the event, the hair most likely originated from an operator during the manufacturing process.
Event or Problem Description
Name of procedure being performed: na incoming inspection.Detailed description of event: [name] incoming inspection po# (b)(6).This is a complaint from [name] evaluation team.The lot mentioned above was found to have defective units per our incoming inspection.Delivery date: (b)(6) 2021.Please refer to the attachment file.Photos are available.Products available for return.Hairlike object in pouch - cff75 lot # 1420215 (1 ea) patient status: na (no patient involvement) type of intervention: na incoming inspection.

• Brand Name: CFF75, 12X75 KII FIOS ADVFIX 6/BX
• Common Device Name: LAPAROSCOPE, GENERAL & PLASTIC SURGERY
• Manufacturer (Section D): APPLIED MEDICAL RESOURCES; 22872 avenida empresa; rancho santa margarita CA 92688
• Manufacturer Contact: aaron fulcher ; 22872 avenida empresa; rancho santa margarita, CA 92688 ; 9497135765
• MDR Report Key: 12579585
• Report Number: 2027111-2021-00659
• Device Sequence Number: 19663671
• Product Code: GCJ
• UDI-Device Identifier: 00607915136659
• UDI-Public: (01)00607915136659(17)240713(30)01(10)1420215
• Combination Product (Y/N): N
• Initial Reporter Country: JA
• PMA/510(K) Number: K083638
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Foreign,Distributor
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date (Section B): 12/03/2021

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
• Device Expiration Date: 07/13/2024
• Device Model Number: CFF75
• Device Catalogue Number: 101471079
• Device Lot Number: 1420215
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 09/28/2021
• Is the Reporter a Health Professional?: No
• Was the Report Sent to FDA?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 09/03/2021
• Supplement Date Received by Manufacturer: 09/03/2021
• Initial Report FDA Received Date: 10/05/2021
• Supplement Report FDA Received Date: 12/03/2021
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 07/14/2021
• 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