MAUDE Adverse Event Report: FERROSAN MEDICAL DEVICES A/S; SURGIFOAM® ABSORBABLE GELATIN POWDER KIT

Medical Device Problem Code	Delivered as Unsterile Product (1421)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Type of Reportable Event	Malfunction
Event or Problem Description
Customer notified rep of issues yet again with 1979.Appeared to be different lot #s than previous complaints.Rep to pick up product and verify.The issue being that the package that the syringe tip comes in is not sealed entirely for sterilization.The customer luckily went through their entire inventory as was able to identify about 10 eaches that this affected.No patient harm.Ten products are available for evaluation.The cases are considered near adverse events (if the event occurred again, it could result in a serious adverse event).2 cases with a total of 14 complaints were received from ethicon's complaint team on (b)(6) 2024 and (b)(6) 2024 respectively.The cases are considered near adverse events per 03.04.2024.Initially, the cases were not evaluated to be near adverse events as the malfunction was discovered prior to surgery.No delay in surgery and no patient harm was reported.As the second complaint was received, and no complaint samples were received from the first complaint, the retained samples for the batch/es were investigated.The investigation revealed that there was a risk for the surgeon/nurse to overlook the comprised sterile barrier and use a possible non-sterile product in a patient.The awareness date is considered as 03.04.2024 as this was the day where the retained samples were investigated and a possible risk for patient harm identified.An investigation is in progress.
Event or Problem Description
Customer notified rep of issues yet again with 1979.Appeared to be different lot #s than previous complaints.Rep to pick up product and verify.The issue being that the package that the syringe tip comes in is not sealed entirely for sterilization.The customer luckily went through their entire inventory as was able to identify about 10 eaches that this affected.No patient harm.Ten products are available for evaluation.Follow-up information was received stating that the is 14 devices (not 10).The cases are considered near adverse events (if the event occurred again, it could result in a serious adverse event).The sterile barrier was compromised.2 cases with a total of 18 complaints were received from ethicon's complaint team on (b)(6) 2024 and (b)(6) 2024 respectively.The cases are considered near adverse events per 03.04.2024.Initially, the cases were not evaluated to be near adverse events as the malfunction was discovered prior to surgery.No delay in surgery and no patient harm was reported.As the second complaint was received, and no complaint samples were received from the first complaint, the retained samples for the batch/es were investigated.The investigation revealed that there was a risk for the surgeon/nurse to overlook the comprised sterile barrier and use a possible non-sterile product in a patient.The awareness date is considered as (b)(6) 2024 as this was the day where the retained samples were investigated and a possible risk for patient harm identified.An investigation is in progress.Follow-up questions/investigation are handled in the complaint qns.Follow-up information confirms the near adverse event (no patient harm).The investigation concluded that the welding of the pouch of the tips (only included in product 1979, powder kit) was defect in 3 batches (only sold in us) and root causes which is being handled as capa.The 3 batches are recalled (2210968-04.23.2024-001-r).

• Common Device Name: SURGIFOAM® ABSORBABLE GELATIN POWDER KIT
• Manufacturer (Section D): FERROSAN MEDICAL DEVICES A/S; sydmarken 5; soeborg, 2860 ; DA 2860
• MDR Report Key: 19114333
• Report Number: 3008478369-2024-00018
• Device Sequence Number: 12717710
• Product Code: LMF
• UDI-Device Identifier: 15712123000264
• UDI-Public: 15712123000264
• Combination Product (Y/N): N
• PMA/510(K) Number: P990004
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Initial Reporter Occupation: Other
• Remedial Action: Recall
• Type of Report: Initial,Followup

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?: No
• Is the Reporter a Health Professional?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: Not provided
• Supplement Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 04/16/2024
• Supplement Report FDA Received Date: 05/08/2024
• Patient Sequence Number: 1
• Patient Sex: Unknown