FDA Adverse Event Injury Summary report: N

AMPLATZER PICCOLO

MDR report key: 17652204 · Received August 30, 2023

Report

Report Number
2135147-2023-03770
Event Type
Injury
Date Received
August 30, 2023
Date of Event
October 12, 2022
Report Date
October 19, 2023
Manufacturer
ABBOTT MEDICAL
Product Code
MAE
UDI-DI
05415067031044
PMA / PMN Number
P020024
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
LA, US
Reporter Occupation
PHYSICIAN
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

AN EVENT OF DIFFICULTY BREATHING WAS REPORTED. FIELD INDICATED THAT ECHOCARDIOGRAM SHOWED OBSTRUCTION ON THE LEFT PULMONARY ARTERY (LPA) DUE TO PATIENT ANATOMY WHICH MAY HAVE CONTRIBUTED TO THE REPORTED EVENT. PATIENT UNDERWENT SURGICAL LPA ANGIOPLASTY. A MORE COMPREHENSIVE ASSESSMENT COULD NOT BE PERFORMED AS THE DEVICE REMAINS IMPLANTED AND WAS NOT RETURNED FOR ANALYSIS. THE DEVICE HISTORY RECORD WAS REVIEWED TO ENSURE THAT EACH MANUFACTURING AND INSPECTION OPERATION WAS PERFORMED, AND THE PRODUCT MET ALL SPECIFICATIONS. BASED ON THE INFORMATION RECEIVED, THE CAUSE OF THE REPORTED INCIDENT COULD NOT BE CONCLUSIVELY DETERMINED. H6 MEDICAL DEVICE PROBLEM CODE: CODE 1395 AND 2017 REMOVED.

Additional Manufacturer Narrative · 0

INVESTIGATION IS NOT YET COMPLETE. A FOLLOW-UP REPORT WILL BE SUBMITTED WITH ALL ADDITIONAL RELEVANT INFORMATION.

Description of Event or Problem · 0

IT WAS REPORTED THAT ON (B)(6) 2022, A 5MM BY 4MM AMPLATZER PICCOLO OCCLUDER (LOT 8421938) WAS CHOSEN FOR IMPLANT, USING A 4F AMPLATZER TORQVUE LP DELIVERY SYSTEM FOR 30 DAYS OLD, 1.2 KG PATIENT WITH THE FOLLOWING PATENT DUCTUS ARTERIOSUS (PDA) MEASUREMENTS: MINIMAL DIAMETER OF 3.5MM, LENGTH OF 11.3MM, AND DIAMETER AT AORTIC AMPULLA OF 4.5MM. IT WAS INDICATED THAT THE PHYSICIAN FELT MEASUREMENTS AND WEIGHT WERE "BORDERLINE" BETWEEN DEVICE CHOICES. PER PHYSICIAN DOWNSIZING WAS NOT AN OPTION. ORIGINAL DEPLOYMENT HAD IMMEDIATE EMBOLIZATION OF THIS DEVICE THAT WAS CONFIRMED IN FLUOROSCOPY, WHICH WAS RETRIEVED VIA 10MM GOOSENECK SNARE, AND REMOVED FROM THE PATIENT. A REPLACEMENT 5MM BY 4MM AMPLATZER PICCOLO OCCLUDER (LOT 8160390) WAS SUCCESSFULLY IMPLANTED WITH SATISFACTORY RESULT PER PHYSICIAN. ON (B)(6) 2022, ECHOCARDIOGRAM SHOWED OBSTRUCTION ON THE LEFT PULMONARY ARTERY (LPA) DUE TO PATIENT ANATOMY. THE PATIENT EXPERIENCED DIFFICULTY BREATHING, REQUIRING RESPIRATORY SUPPORT. THE PATIENT UNDERWENT MEDICAL INTERVENTION; HOWEVER, THE PHYSICIAN WAS UNABLE TO CROSS INTO THE LPA. ON (B)(6) 2022, THE PATIENT UNDERWENT SURGICAL LPA ANGIOPLASTY. THE PATIENT WAS DISCHARGED AND REPORTED TO BE STABLE.

Description of Event or Problem · 0

IT WAS REPORTED THAT ON (B)(6) 2022, A 5MM BY 4MM AMPLATZER PICCOLO OCCLUDER WAS SUCCESSFULLY IMPLANTED USING A 4F AMPLATZER TORQVUE LP DELIVERY SYSTEM FOR A 1.2 KG PATIENT WITH THE FOLLOWING PATENT DUCTUS ARTERIOSUS (PDA) MEASUREMENTS: MINIMAL DIAMETER OF 3.5MM, LENGTH OF 11.3MM, AND DIAMETER AT AORTIC AMPULLA OF 4.5MM. IT WAS INDICATED THAT THE PHYSICIAN FELT MEASUREMENTS AND WEIGHT WERE "BORDERLINE" BETWEEN DEVICE CHOICES. PER PHYSICIAN DOWNSIZING WAS NOT AN OPTION. ORIGINAL DEPLOYMENT HAD IMMEDIATE EMBOLIZATION OF THIS DEVICE, WHICH WAS RECAPTURED AND REPOSITIONED WITH SATISFACTORY RESULTS PER PHYSICIAN. ON (B)(6) 2022, ECHOCARDIOGRAM SHOWED OBSTRUCTION ON THE LEFT PULMONARY ARTERY (LPA) DUE TO PATIENT ANATOMY. THE PATIENT EXPERIENCED DIFFICULTY BREATHING, REQUIRING RESPIRATORY SUPPORT. THE PATIENT UNDERWENT MEDICAL INTERVENTION; HOWEVER, THE PHYSICIAN WAS UNABLE TO CROSS INTO THE LPA. ON (B)(6) 2022, THE PATIENT UNDERWENT SURGICAL LPA ANGIOPLASTY. THE PATIENT WAS DISCHARGED AND REPORTED TO BE STABLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1315827 AMPLATZER PICCOLO OCCLUDER, PATENT DUCTUS, ARTERIOSUS MAE ABBOTT MEDICAL 8160390 05415067031044

Patients

Seq Age Sex Outcome Treatment
1 30 DA Male Hospitalization| R