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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: SMITH & NEPHEW, INC. INTEGRAL BIPOLAR CUP SET 38MM; HIP PROSTHESIS
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SMITH & NEPHEW, INC. INTEGRAL BIPOLAR CUP SET 38MM; HIP PROSTHESIS Back to Search Results
Catalog Number 11138
Device Problem Migration or Expulsion of Device (1395)
Patient Problem No Code Available (3191)
Event Date 11/26/2015
Event Type  Injury  
Manufacturer Narrative
Customer indicated that there is no product/device to be returned for investigation analysis.
 
Event Description
It was reported that a revision surgery was performed due to cup migration into pelvis.
 
Manufacturer Narrative
The associated complaint devics were not returned.Without the actual products involved and/or device information, our investigation cannot proceed.If the devices or new information is received in the future, this complaint can be re-opened.No further actions are being taken at this time.
 
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Brand Name
INTEGRAL BIPOLAR CUP SET 38MM
Type of Device
HIP PROSTHESIS
Manufacturer (Section D)
SMITH & NEPHEW, INC.
1450 brooks road
memphis TN 38116
Manufacturer (Section G)
SMITH & NEPHEW, INC.
1450 brooks road
memphis TN 38116
Manufacturer Contact
robert rust
1450 brooks road
memphis, TN 38116
9013991624
MDR Report Key5321991
MDR Text Key34198239
Report Number1020279-2015-00873
Device Sequence Number1
Product Code JDH
Combination Product (y/n)N
Reporter Country CodeJA
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type company representative,foreig
Reporter Occupation Physician
Type of Report Initial,Followup
Report Date 12/02/2015
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received12/23/2015
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Device Operator Health Professional
Device Catalogue Number11138
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? Yes
Date Manufacturer Received12/02/2015
Was Device Evaluated by Manufacturer? Device Not Returned to Manufacturer
Is the Device Single Use? Yes
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Initial
Patient Sequence Number1
Patient Outcome(s) Hospitalization; Required Intervention;
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