• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE Adverse Event Report: HEARTSINE TECHNOLOGIES LTD PACKAGE, 350P, PP03, UK, 350-STR-UK-10; AUTOMATED EXTERNAL DEFIBRILLATOR

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

HEARTSINE TECHNOLOGIES LTD PACKAGE, 350P, PP03, UK, 350-STR-UK-10; AUTOMATED EXTERNAL DEFIBRILLATOR Back to Search Results
Model Number SAM350P
Medical Device Problem Codes Failure to Power Up (1476); Electrical Power Problem (2925)
Health Effect - Clinical Code No Clinical Signs, Symptoms or Conditions (4582)
Date of Event 09/10/2021
Type of Reportable Event Malfunction
Additional Manufacturer Narrative
Heartsine has requested return of the device for investigation.Upon completion, the conclusions will be submitted in a follow-up report.
 
Event or Problem Description
Failure to power on device may prevent or delay defibrillation, which could cause an adverse event.No patient involvement.
 
Event or Problem Description
The distributor contacted heartsine to report that their device was failing to power on.Failure to power on device may prevent or delay defibrillation, which could cause an adverse event.There was no patient involvement reported with this event.
 
Additional Manufacturer Narrative
Heartsine has made multiple attempts to contact the customer regarding the status of their device, but no response has been received from the customer.The device was not returned to heartsine for investigation.No additional information will be forthcoming at this time.The cause of the reported issue could not be determined.If the device is returned to the manufacturer the investigation will be reopened.H3 other text : device not returned for evaluation.
 
Event or Problem Description
The distributor contacted heartsine to report that their device was failing to power on.Failure to power on device may prevent or delay defibrillation, which could cause an adverse event.There was no patient involvement reported with this event.
 
Additional Manufacturer Narrative
Heartsine's investigation of the device confirmed the reported fault, as upon receipt the device was observed to be switching on automatically as well as being unable to switch off.The fault was attributed to corrosion on the membrane tail, due to storage outside of the indicated conditions.The device was scrapped by heartsine and the customer was provided with a replacement device.
 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand Name
PACKAGE, 350P, PP03, UK, 350-STR-UK-10
Common Device Name
AUTOMATED EXTERNAL DEFIBRILLATOR
Manufacturer (Section D)
HEARTSINE TECHNOLOGIES LTD
207 airport road west
belfast BT3 9 ED
EI  BT3 9ED
Manufacturer (Section G)
HEARTSINE TECHNOLOGIES LTD
207 airport road west
belfast BT3 9 ED
EI   BT3 9ED
Manufacturer Contact
todd bandy
207 airport road west
belfast BT3 9-ED
EI   BT3 9ED
4258674577
MDR Report Key12466194
Report Number3004123209-2021-00234
Device Sequence Number3687385
Product Code MKJ
UDI-Device IdentifierM727SAM350P
UDI-PublicM727SAM350P
Combination Product (Y/N)N
Initial Reporter CountryEI
PMA/510(K) Number
P160008
Number of Events Summarized1
Summary Report (Y/N)N
Reporter Type Manufacturer
Report Source Distributor
Initial Reporter Occupation Other
Type of Report Initial,Followup,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
Operator of Device Lay User/Patient
Device Model NumberSAM350P
Device Catalogue Number350-STR-UK-10
Was Device Available for Evaluation? Device Returned to Manufacturer
Date Returned to Manufacturer11/08/2021
Is the Reporter a Health Professional? No
Type of Report(Section G)Follow-Up
Initial Date Received by Manufacturer 09/10/2021
Supplement Date Received by Manufacturer11/02/2021
12/01/2021
Initial Report FDA Received Date09/14/2021
Supplement Report FDA Received Date11/03/2021
12/03/2021
Was Device Evaluated by Manufacturer? (Y/N) Yes
Date Device Manufactured10/20/2016
Is the Device Labeled for Single Use? (Y/N) No
Is This a Single-Use Device that was
Reprocessed and Reused on a Patient? (Y/N)
No
Usage of Device Reuse
Patient Sequence Number1
Patient SexUnknown
-
-