MAUDE Adverse Event Report: CORDIS CORPORATION SABER035; CATHETER, ANGIOPLASTY, PERIPHERAL, TRANSLUMINAL

Catalog Number	48007004N
Medical Device Problem Code	Burst Container or Vessel (1074)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	11/14/2024
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
Additional information is pending and will be submitted within 30 days upon receipt.
Event or Problem Description
As reported, two.035 7x40 saber percutaneous transluminal angioplasty (pta) balloons burst while hand inflation was being performed.The pta balloons were removed and additional third balloon was used at lesion.The third balloon was used to finish the case.There was no reported injury to the patient.The product was opened and prepped in the sterile field per the instructions for use (ifu).The balloons were inserted through the unknown sheath and advanced to the target lesion.The devices will be returned for evaluation.
Event or Problem Description
As reported, two.035 7x40 saber percutaneous transluminal angioplasty (pta) balloons burst while hand inflation was being performed.The pta balloons were removed and additional third balloon was used at lesion.The third balloon was used to finish the case.There was no reported injury to the patient.The product was opened and prepped in the sterile field per the instructions for use (ifu).The balloons were inserted through the unknown sheath and advanced to the target lesion.Additional information and device return was requested; however, neither were not obtained after multiple attempts made.
Additional Manufacturer Narrative
As reported, two.035 7x40 saber percutaneous transluminal angioplasty (pta) balloons burst while hand inflation was being performed.The pta balloons were removed and additional third balloon was used at lesion.The third balloon was used to finish the case.There was no reported injury to the patient.The product was opened and prepped in the sterile field per the instructions for use (ifu).The balloons were inserted through the unknown sheath and advanced to the target lesion.Additional information was request but was not obtained after multiple attempts made.The reported ¿balloon burst ¿ for both complaints could not be confirmed as the device was not returned for analysis.The exact cause could not be determined.Without return of the product for analysis or films of the event it is difficult to draw a clinical conclusion between the device and the reported event.Anatomical, procedural, and/or handling factors could all have contributed to the reported issues.According to the warnings in the safety information in the instructions for use, ¿prior to angioplasty, the catheter should be examined to verify functionality and integrity, and ensure that its size and shape are suitable for the specific procedure for which it is to be used.Do not use if product damage is suspected or evident.To reduce the potential for vessel damage or the risk of dislodgement of particles it is very important that the inflated diameter of the balloon should approximate the diameter of the vessel just proximal and distal to the lesion.The balloon dimensions are printed on the product label.The compliance table incorporated with the product shows how balloon diameter increases as pressure increases.Do not exceed the rated burst pressure recommended on the label.The rated burst pressure is based on the results of in vitro testing.At least (b)(4) of the balloons (with a (b)(4) confidence) will not burst at or below their rated burst pressure.Use of a pressure monitoring device is recommended to prevent over-pressurization.Pressure in excess of the rated burst pressure can cause balloon rupture and potential inability to withdraw the catheter through the introducer sheath.Balloon rupture can cause vessel damage and the need for additional intervention.Use only the recommended balloon inflation medium (a 50/50 mixture by volume of contrast medium and normal saline).Never use air or any gaseous medium to inflate the balloon.¿ the information available does not suggest a design or manufacturing related cause for the reported event.Therefore, no corrective or preventive action will be taken at this time.

• Brand Name: SABER035
• Common Device Name: CATHETER, ANGIOPLASTY, PERIPHERAL, TRANSLUMINAL
• Manufacturer (Section D): CORDIS CORPORATION; 14201 nw 60 avenue nw 60 avenue; miami lakes FL 33014
• Manufacturer (Section G): CORDIS US CORP.; 14201 nw 60 avenue; miami lakes FL 33014
• Manufacturer Contact: karla castro ; coyol free zone, building b25, , , costa rica; el coyol alajuela bld 25 ; 7863138372
• MDR Report Key: 20880257
• Report Number: 3007635982-2024-00285
• Device Sequence Number: 8843035
• Product Code: LIT
• UDI-Device Identifier: 20705032079881
• UDI-Public: (01)20705032079881(17)260131(10)82275141
• Combination Product (Y/N): N
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): Unknown
• Reporter Type: Manufacturer
• Report Source: Health Professional,Company Representative
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 12/18/2024

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: 01/31/2026
• Device Catalogue Number: 48007004N
• Device Lot Number: 82275141
• 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: Not provided
• Supplement Date Received by Manufacturer: 12/16/2024
• Initial Report FDA Received Date: 12/09/2024
• Supplement Report FDA Received Date: 12/18/2024
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 02/13/2023
• 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