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

MAUDE Adverse Event Report: GETINGE DISINFECTION AB 88-SERIES; MEC

  • 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
 

GETINGE DISINFECTION AB 88-SERIES; MEC Back to Search Results
Model Number 88-5
Device Problem Component Falling (1105)
Patient Problem No Patient Involvement (2645)
Event Date 08/26/2015
Event Type  malfunction  
Manufacturer Narrative
During review of complaints performed on 12th june 2017 for one of the reportable cases we became aware of the similar issues which have been registered in our internal system in the past.As the revision of the recorded information shown that previous cases were similar we decided to report it retrospectively.The malfunction occurred on a air glide system (ags) called unloading conveyor.This is not a medical device.It is an accessory to getinge 88-series and 86-series washer disinfector device.The conveyor loads and unloads racks with material to be disinfected, into and out of the disinfector.That it is all it does and in that way it has no effect on the core performance of the disinfector device.Getinge received customer complaint where the cart transferred from the washer disinfector was pushed out from the shuttle and as a result crashed on the floor.No information about operators was provided.It was established that when the event occurred the unloader working in the system with the washer-disinfector device has not met its specification and it contributed to the event.When the event occurred the device was being used by the user.During the investigation it was found that the event occurred as a result of two factors: the program needs an override action to be performed by the user, by the pressing the reset button.The reset is done by the operator if the cart is not moved to the unloader from the washer disinfector or any other problem with the cart transferring.The end pin of the unloader needs to be stuck in the down position.When the pin is in down position there is no mechanical protection to keep the cart on the conveyor, therefore when the cart reaches the edge of the conveyor is not mechanically stopped and it falls off.It was concluded that when both of mentioned factors appear in the same time the cart could not be stopped at the end of the conveyor and could fall down on the floor.(b)(4).
 
Event Description
On (b)(6) 2015 getinge received customer complaint of the incident where the cart transferred from the washer disinfector was pushed out from the shuttle and as a result crashed on the floor.No information about operators was provided.
 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand Name
88-SERIES
Type of Device
MEC
Manufacturer (Section D)
GETINGE DISINFECTION AB
ljungadalsgatan 11
vaxjo kronobergs ian [se-07]
vaxjo, 35115
SW  35115
Manufacturer (Section G)
GETINGE DISINFECTION AB
ljungadalsgatan 11
vaxjo kronobergs ian [se-07]
35115
SW   35115
Manufacturer Contact
ann wheeler
1777 e. henrietta road
rochester, NY 14623
5852725036
MDR Report Key6704294
MDR Text Key79798497
Report Number9616031-2017-00021
Device Sequence Number1
Product Code MEC
Combination Product (y/n)N
Reporter Country CodeNO
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type user facility
Reporter Occupation Other Health Care Professional
Remedial Action Repair
Type of Report Initial
Report Date 07/11/2017
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received07/11/2017
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Other Health Care Professional
Device Model Number88-5
Was Device Available for Evaluation? Yes
Is the Reporter a Health Professional? Yes
Was the Report Sent to FDA? Yes
Date Report Sent to FDA07/11/2017
Device Age10 MO
Event Location Hospital
Date Report to Manufacturer07/11/2017
Date Manufacturer Received06/12/2017
Was Device Evaluated by Manufacturer? Yes
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Reuse
Patient Sequence Number1
Patient Outcome(s) Other;
-
-