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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: SMITH & NEPHEW, INC. TANDEM UNI CONV TRL 0MM; ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

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SMITH & NEPHEW, INC. TANDEM UNI CONV TRL 0MM; ORTHOPEDIC MANUAL SURGICAL INSTRUMENT Back to Search Results
Model Number 71367900
Medical Device Problem Code Connection Problem (2900)
Health Effect - Clinical Code No Known Impact Or Consequence To Patient (2692)
Date of Event 06/19/2020
Type of Reportable Event Serious Injury
Event or Problem Description
It was reported that during total hip replacement the unipolar trial heads do not stay on the stem or broach trials.It was tried all 5 devices and the pop off non stop.A delay was reported of 10 minutes to 15 minutes.The procedure was finished using a change in the surgical technique.A different device has to be used to finished the procedure.The procedure was finished using 28 mm bipolar head.
 
Additional Manufacturer Narrative
Additional information in g4, h6 investigation results: the device used in treatment was returned for evaluation.Visual inspection of the returned device confirms that the device has wear and tear in the inner rim of the trial head which is not allowing the device to stay in place.A complaint history review found related failures; this failure mode will be monitored for future complaints for any necessary corrective actions.According to clinical/medical investigation, the unipolar trial heads would not stay on the stem or broach trials.Reportedly, ¿the patient is fine, the procedure was finished using a change in the surgical technique¿.A different device had to be used to finished the procedure.Smith and nephew has not received adequate materials to fully evaluate the complaint, but if additional clinically relevant materials are later received, then the case may be re-opened for further evaluation.At this time, we have no reason to suspect that the product failed to meet any product specifications at the time of manufacture.The device is a reusable device that can be exposed to numerous surgeries and cleaning cycles.Probable causes that could contribute to the reported event, as reusable instruments are susceptible to damage from prolonged use and through misuse or rough handling.To avoid compromised performance or damage, it is recommended the device be inspected prior to and after each use and cleaning.We recommend that all re-usable instruments be routinely inspected for wear/damage and replaced as necessary.A review of risk management files and the instructions for use found that the reported failure was documented appropriately.Based on this investigation, the need for corrective action is not indicated.Should additional information be received, the complaint will be reopened.No further actions are being taken at this time.We consider this investigation closed.
 
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Brand Name
TANDEM UNI CONV TRL 0MM
Common Device Name
ORTHOPEDIC MANUAL SURGICAL INSTRUMENT
Manufacturer (Section D)
SMITH & NEPHEW, INC.
1450 brooks rd.
memphis TN 38116
MDR Report Key10293443
Report Number1020279-2020-03323
Device Sequence Number13655822
Product Code LXH
UDI-Device Identifier03596010481733
UDI-Public03596010481733
Combination Product (Y/N)N
Initial Reporter CountryUS
PMA/510(K) Number
EXEMPT
Number of Events Summarized1
Summary Report (Y/N)N
Reporter Type Manufacturer
Report Source health professional,user faci
Initial Reporter Occupation Other Health Care Professional
Type of Report Initial,Followup
Report Date (Section B) 04/14/2021
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? Yes
Operator of Device Health Professional
Device Model Number71367900
Device Catalogue Number71367900
Device Lot NumberUNKNOWN
Initial Date Received by Manufacturer 06/22/2020
Supplement Date Received by Manufacturer04/01/2021
Initial Report FDA Received Date07/18/2020
Supplement Report FDA Received Date04/14/2021
Is This a Single-Use Device that was
Reprocessed and Reused on a Patient? (Y/N)
No
Patient Sequence Number1
Outcome Attributed to Adverse Event Required Intervention;
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