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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: MAQUET SAS BLUELINE; LIGHT, SURGICAL, CEILING MOUNTED

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MAQUET SAS BLUELINE; LIGHT, SURGICAL, CEILING MOUNTED Back to Search Results
Catalog Number HM56077460
Device Problem Contamination /Decontamination Problem (2895)
Patient Problem No Clinical Signs, Symptoms or Conditions (4582)
Event Date 03/29/2023
Event Type  malfunction  
Manufacturer Narrative
Additional information will be provided following the conclusion of the investigation.Device not returned to manufacturer.
 
Event Description
On (b)(6) 2023, getinge became aware of an issue with one of surgical lights - blueline.Based on photographic evidence the accumulation of particles was found on the connection of the spring arm with fork.We decided to report the issue in abundance of caution as any particles falling off into sterile field or during procedure may cause contamination.
 
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Brand Name
BLUELINE
Type of Device
LIGHT, SURGICAL, CEILING MOUNTED
Manufacturer (Section D)
MAQUET SAS
parc de limere
avenue de la pomme de pin
ardon
Manufacturer (Section G)
MAQUET SAS
parc de limere
avenue de la pomme de pin
ardon
Manufacturer Contact
pascal jay
parc de limere
avenue de la pomme de pin
ardon 
MDR Report Key16749628
MDR Text Key313397853
Report Number9710055-2023-00308
Device Sequence Number1
Product Code FSY
Combination Product (y/n)N
Reporter Country CodeGM
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type Foreign,User Facility,Company Representative
Reporter Occupation Other
Type of Report Initial
Report Date 04/17/2023
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 Catalogue NumberHM56077460
Was Device Available for Evaluation? Yes
Initial Date Manufacturer Received 03/29/2023
Initial Date FDA Received04/17/2023
Was Device Evaluated by Manufacturer? No
Date Device Manufactured04/11/2007
Is the Device Single Use? No
Type of Device Usage Reuse
Patient Sequence Number1
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