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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: AIZU OLYMPUS CO., LTD. TRACHEAL INTUBATION FIBERSCOPE
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AIZU OLYMPUS CO., LTD. TRACHEAL INTUBATION FIBERSCOPE Back to Search Results
Model Number LF-DP
Device Problem Peeled/Delaminated (1454)
Patient Problem No Clinical Signs, Symptoms or Conditions (4582)
Event Type  malfunction  
Event Description
It was observed that during the device evaluation, the intubation fiberscope exhibited a peeled coating of the image guide hose.There were no reports of patient involvement.
 
Manufacturer Narrative
The device evaluation is ongoing.Should additional relevant information become available, a supplemental report will be submitted.
 
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Brand Name
TRACHEAL INTUBATION FIBERSCOPE
Type of Device
TRACHEAL INTUBATION FIBERSCOPE
Manufacturer (Section D)
AIZU OLYMPUS CO., LTD.
3-1-1 niiderakita
aizuwakamatsu-shi, fukushima 965-8 520
JA  965-8520
Manufacturer (Section G)
AIZU OLYMPUS CO., LTD.
3-1-1 niiderakita
aizuwakamatsu-shi, fukushima 965-8 520
JA   965-8520
Manufacturer Contact
todd brill
800 west park drive
westborough, MA 01581
5082077661
MDR Report Key19194330
MDR Text Key341181910
Report Number9610595-2024-08760
Device Sequence Number1
Product Code EOQ
UDI-Device Identifier04953170059032
UDI-Public04953170059032
Combination Product (y/n)N
Reporter Country CodeJA
PMA/PMN Number
K981543
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type Foreign,Company Representative
Reporter Occupation Non-Healthcare Professional
Type of Report Initial
Report Date 04/26/2024
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received04/26/2024
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Other
Device Model NumberLF-DP
Was Device Available for Evaluation? Device Returned to Manufacturer
Date Returned to Manufacturer04/04/2024
Was the Report Sent to FDA? No
Date Manufacturer Received04/12/2024
Was Device Evaluated by Manufacturer? No
Date Device Manufactured04/22/2014
Is the Device Single Use? No
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Reuse
Patient Sequence Number1
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