FDA Adverse Event Malfunction Summary report: N

BREASTPUMP PNSA STARTER

MDR report key: 6090421 · Received November 9, 2016

Report

Report Number
1419937-2016-00289
Event Type
Malfunction
Date Received
November 9, 2016
Date of Event
November 7, 2016
Report Date
November 7, 2016
Manufacturer
MEDELA INC
Product Code
HGX
PMA / PMN Number
K031614
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IL, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE CUSTOMER WAS SENT A REPLACEMENT POWER ADAPTER. THE PRODUCT INVOLVED IN THE COMPLAINT WAS NOT RETURNED FOR EVALUATION/INVESTIGATION AT THIS TIME. THEREFORE, NO CONCLUSIONS CAN BE MADE AS TO THE CAUSE OF THE EVENT. THIS ISSUE WITH THE DAMAGED TRANSFORMER HOUSING FOR THE PUMP IN STYLE DEVICE WAS ADDRESSED IN INVESTIGATION (B)(4). THE INVESTIGATION FOUND THAT THE TRANSFORMERS ARE BEING DAMAGED DURING SHIPMENT FROM THE MANUFACTURER TO MEDELA. THIS DAMAGE IS CAUSING THE PLASTIC HOUSING TO FAIL PREMATURELY WHEN SUBJECTED TO NORMAL USE AND FORESEEABLE MISUSE. THE PACKAGING USED BY THE MANUFACTURER TO SHIP THE TRANSFORMERS TO MEDELA IS NOT ROBUST ENOUGH TO HANDLE ALL OF THE POTENTIAL SHIPPING, HANDLING, AND ABUSE CONDITIONS THAT COULD ARISE FROM LOGISTICS OF THE CONSOLIDATION PROCESS. AS A RESULT OF THE INVESTIGATION, THE SHIPPING AND CONSOLIDATION PROCESS HAS BEEN MODIFIED TO REDUCE THE HANDLING AND POTENTIAL FOR DOUBLE STACKING OF THE SKIDS. THE SHIPPING PACKAGING STRENGTH HAS ALSO BEEN INCREASED TO FURTHER PROTECT THE TRANSFORMERS DURING SHIPPING. COMPLAINTS AGAINST THIS PRODUCT ARE CURRENTLY BEING MONITORED FOR EFFECTIVENESS OF THE ABOVE MENTIONED CORRECTIVE ACTION.

Description of Event or Problem · 1

THE CUSTOMER REPORTED TO CUSTOMER SERVICE ON (B)(6) 2016, THAT THE POWER ADAPTER TO HER PUMP IN STYLE ADVANCED BREASTPUMP HAD BROKE AND CRACKED OPEN WHEN PULLING IT OUT OF THE WALL OUTLET.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
742589 BREASTPUMP PNSA STARTER PUMP, BREAST, POWERED HGX MEDELA INC 9207010/57081 REV M - 1512

Patients

Seq Age Sex Outcome Treatment
1