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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: GOODBABY 3 POSITION RECLINER DELUXE-X WIDE ROSEWOOD 9153641330; CHAIR AND TABLE, MEDICAL

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GOODBABY 3 POSITION RECLINER DELUXE-X WIDE ROSEWOOD 9153641330; CHAIR AND TABLE, MEDICAL Back to Search Results
Model Number IH6065A/IH68
Device Problem Break (1069)
Patient Problem No Consequences Or Impact To Patient (2199)
Event Type  malfunction  
Event Description
Per provider, the locking casters are not working.
 
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Brand Name
3 POSITION RECLINER DELUXE-X WIDE ROSEWOOD 9153641330
Type of Device
CHAIR AND TABLE, MEDICAL
Manufacturer (Section D)
GOODBABY
CH 
MDR Report Key4507443
MDR Text Key16635626
Report Number1531186-2015-00925
Device Sequence Number1
Product Code KMN
Combination Product (y/n)N
Reporter Country CodeUS
Number of Events Reported1
Summary Report (Y/N)N
Report Source Distributor
Source Type Invalid Data
Reporter Occupation Medical Equipment Company Technician/Representative
Type of Report Initial
Report Date 02/11/2015,02/05/2015
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received02/11/2015
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Lay User/Patient
Device Model NumberIH6065A/IH68
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? No
Was the Report Sent to FDA? Yes
Date Report Sent to FDA02/11/2015
Distributor Facility Aware Date02/05/2015
Device Age1 YR
Date Report to Manufacturer02/11/2015
Is This a Reprocessed and Reused Single-Use Device? No
Patient Sequence Number1
Patient Outcome(s) Other;
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