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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: JOHNSON & JOHNSON MEDICAL (SUZHOU) LTD.3006356043 ANGLED ACET INSERTR; HIP INSTRUMENT/TRIAL

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JOHNSON & JOHNSON MEDICAL (SUZHOU) LTD.3006356043 ANGLED ACET INSERTR; HIP INSTRUMENT/TRIAL Back to Search Results
Catalog Number 920010029
Device Problem Failure to Disconnect (2541)
Patient Problem No Information (3190)
Event Date 11/24/2015
Event Type  malfunction  
Manufacturer Narrative
This complaint is still under investigation.Depuy will notify the fda of the results of this investigation once it has been completed.(b)(4).If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.
 
Event Description
The surgeon could not remove the inserter from the cup after impacting the cup although the connection between all the trial cups and the inserter had been checked before the surgery.It was reported that they could remove the devices in the pre-op inspection even though the devices were tightened.The surgeon replaced the reported cup with a multi hole cup and completed the surgery with a 25-minute delay.There was no harm to the patient.
 
Manufacturer Narrative
The complaint states during tha for oa on november 24th, the surgeon could not remove the inserter from the cup after impacting the cup although the connection between all the trial cups and the inserter had been checked before the surgery.It was reported that they could remove the devices in the pre-op inspection even though the devices were tightened.The surgeon replaced the reported cup with a multi hole cup and completed the surgery with a 25-minute delay.There was no harm to the patient.The investigation confirmed that the end part of the macs inserter was stuck in the returned cup.In an attempt to solve the issue of the cup sticking to the adaptor the testing of prototype designs created under (b)(4) took place, and research and development report l740 was created.The testing showed that the prototype designs reduced the frequency of locking between the cup and adaptor during testing, but did not eliminate the fundamental cause of sticking.Other designs of introducers have the same issue of sticking.The complaint shall be closed with a justified conclusion; entered into the complaints database and monitored through trend analysis.If further information is received the complaint shall be reopened and investigated further.Depuy still considers the investigation closed at this time.Should additional information be received, the information will be reviewed and the investigation will be re-opened as necessary.
 
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Brand Name
ANGLED ACET INSERTR
Type of Device
HIP INSTRUMENT/TRIAL
Manufacturer (Section D)
JOHNSON & JOHNSON MEDICAL (SUZHOU) LTD.3006356043
no.299 changyang st
suzhou industrial park
suzhou, jiangsu 21512 -6
CH  21512-6
Manufacturer (Section G)
JOHNSON & JOHNSON MEDICAL (SUZHOU) LTD.3006356043
no.299 changyang st
suzhou industrial park
suzhou, jiangsu 21512 -6
CH   21512-6
Manufacturer Contact
chad gibson
700 orthopaedic drive
warsaw, IN 46581
5743725905
MDR Report Key5266887
MDR Text Key32667593
Report Number1818910-2015-36637
Device Sequence Number1
Product Code HWR
Combination Product (y/n)N
Reporter Country CodeUS
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type foreign,health professional
Reporter Occupation Health Professional
Type of Report Initial,Followup
Report Date 11/24/2015
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received12/04/2015
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Health Professional
Device Catalogue Number920010029
Device Lot NumberP00978001
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? Yes
Date Manufacturer Received01/14/2016
Was Device Evaluated by Manufacturer? Device Not Returned to Manufacturer
Date Device Manufactured05/27/2005
Is the Device Single Use? No
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Unknown
Patient Sequence Number1
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