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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: NIHON KOHDEN CORPORATION ORG-9100A; MULTIPLE PATIENT RECEIVER

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NIHON KOHDEN CORPORATION ORG-9100A; MULTIPLE PATIENT RECEIVER Back to Search Results
Model Number ORG-9100A
Device Problems Signal Artifact/Noise (1036); Output Problem (3005)
Patient Problem No Clinical Signs, Symptoms or Conditions (4582)
Event Date 12/23/2021
Event Type  malfunction  
Event Description
The biomedical engineer (bsm) reported that the multiple patient receiver (org) keeps getting a signal loss from one transmitter while monitoring a patient in their room.The bme swapped to a different transmitter but the issue is still there.No patient harm was reported.Nihon kohden technician advised the bme that it is likely the receiver card in the org and recommended that they send in the org for repair.Customer declined returning the org to nihon kohden.
 
Manufacturer Narrative
The biomedical engineer (bsm) reported that the multiple patient receiver (org) keeps getting a signal loss from one transmitter while monitoring a patient in their room.The bme swapped to a different transmitter but the issue is still there.No patient harm was reported.Nihon kohden technician advised the bme that it is likely the receiver card in the org and recommended that they send in the org for repair.Customer declined returning the org to nihon kohden.Nihon kohden continues to investigate the reported event.Nihon kohden will submit a supplemental report in accordance with 21 cfr section 803.56 when additional information becomes available.Additional device information: concomitant medical device: the following device(s) was used in conjunction with the org: zm transmitters: model #: zm-530pa.Serial #: (b)(4).Device manufacturer data: 03/01/2017.Unique identifier (udi) #: (b)(4).
 
Manufacturer Narrative
The biomedical engineer (bsm) reported that the multiple patient receiver (org) keeps getting a signal loss from one transmitter while monitoring a patient in their room.The bme swapped to a different transmitter but the issue is still there.No patient harm was reported.Nihon kohden technician advised the bme that it is likely the receiver card in the org and recommended that they send in the org for repair.Customer declined returning the org to nihon kohden.Investigation summary: customer declined a loaner org and reported this org no longer needs repair.The customer did not provide information on how the issue of communication loss was resolved.No further issues were reported for the org-9100a s/n 271.Root cause cannot be determined.As resolution did not involve assistance from nka, the issue is unlikely to be a result of an nk device malfunction.The root cause for the communication loss is most likely related to customer network environment.As the issue of communication loss could not be confirmed to be cause by a device malfunction and no further issues were reported following this event, a corrective and or preventative action (capa) is not warranted.The following fields are not applicable (na) to this report: the following field(s) contain no information (ni), as attempts to obtain information were made, but not provided: attempt # 1: 01/06/2022 customer called and informed nihon kohden technical support that they will not be returning the org and do not want the loaner org sent to them.Did not provide any further information on the status of the device.Attempt # 2: 01/16/2022 emailed the customer via microsoft outlook for patient information: no reply was received.Attempt # 3: 01/17/2022 emailed the customer via microsoft outlook for patient information: no reply was received.Additional device information: d10 concomitant medical device: the following device(s) was used in conjunction with the org: zm transmitters: model #: zm-530pa.Serial #: (b)(6).Device manufacturer data: 03/01/2017.Unique identifier (udi) #: (b)(4).
 
Event Description
The biomedical engineer (bsm) reported that the multiple patient receiver (org) keeps getting a signal loss from one transmitter while monitoring a patient in their room.The bme swapped to a different transmitter but the issue is still there.No patient harm was reported.Nihon kohden technician advised the bme that it is likely the receiver card in the org and recommended that they send in the org for repair.Customer declined returning the org to nihon kohden.
 
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Brand Name
ORG-9100A
Type of Device
MULTIPLE PATIENT RECEIVER
Manufacturer (Section D)
NIHON KOHDEN CORPORATION
attn: shama mooman
1-31-4 nishiochia
shinjuku-ku, tokyo 161-8 560
JA  161-8560
Manufacturer (Section G)
NIHON KOHDEN TOMIOKA CORPORATION
attn: shama mooman
1-1 tajino
tomioka city, gunma 370-2 314
JA   370-2314
Manufacturer Contact
shama mooman
safety mgmt dept, quality mgmt
seibu bldg 2, 4th floor 1-11-2
kusunokidai tokorozawa, saitama 359-8-580
JA   359-8580
MDR Report Key13266565
MDR Text Key288833860
Report Number8030229-2022-02393
Device Sequence Number1
Product Code DRG
UDI-Device Identifier04931921103883
UDI-Public04931921103883
Combination Product (y/n)N
Reporter Country CodeUS
PMA/PMN Number
K071058
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type Health Professional,User Facility
Reporter Occupation Biomedical Engineer
Type of Report Initial,Followup
Report Date 06/22/2022
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 Operator Health Professional
Device Model NumberORG-9100A
Device Catalogue NumberORG-9100A
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? Yes
Initial Date Manufacturer Received 12/23/2021
Initial Date FDA Received01/17/2022
Supplement Dates Manufacturer Received06/07/2022
Supplement Dates FDA Received06/22/2022
Was Device Evaluated by Manufacturer? Device Not Returned to Manufacturer
Date Device Manufactured12/17/2009
Is the Device Single Use? No
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Reuse
Patient Sequence Number1
Treatment
ZM TRANSMITTERS; ZM TRANSMITTERS
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