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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: SMITH & NEPHEW, INC. ARTICULAR SURFACE PROVISIONAL SZ 3 9MM; TEMPLATE
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SMITH & NEPHEW, INC. ARTICULAR SURFACE PROVISIONAL SZ 3 9MM; TEMPLATE Back to Search Results
Catalog Number 00584102309
Medical Device Problem Code Break (1069)
Health Effect - Clinical Code No Consequences Or Impact To Patient (2199)
Date of Event 02/19/2019
Type of Reportable Event Malfunction
Event or Problem Description
It was reported that the poly insert trial snapped when removed after trailing.No delay and no back-up device was available.No injury involved.
 
Additional Manufacturer Narrative
The associated complaint device was not returned.We recommend that all re-usable instruments be routinely inspected for wear/damage and replaced as necessary.Without the actual device involved our investigation cannot proceed.If the device or new information is received in the future, the complaints can be re-opened.No further actions are being taken at this time.We consider this investigation closed.
 
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Brand Name
ARTICULAR SURFACE PROVISIONAL SZ 3 9MM
Common Device Name
TEMPLATE
Manufacturer (Section D)
SMITH & NEPHEW, INC.
1450 brooks road
memphis TN 38116
MDR Report Key8410173
Report Number1020279-2019-01039
Device Sequence Number1811195
Product Code HWT
UDI-Device Identifier00885556619452
UDI-Public00885556619452
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 company representative,health
Initial Reporter Occupation Physician
Type of Report Initial,Followup
Report Date (Section B) 06/15/2019
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Operator of Device Health Professional
Device Catalogue Number00584102309
Initial Date Received by Manufacturer 02/19/2019
Supplement Date Received by Manufacturer06/14/2019
Initial Report FDA Received Date03/11/2019
Supplement Report FDA Received Date06/15/2019
Is This a Single-Use Device that was
Reprocessed and Reused on a Patient? (Y/N)		 No
Patient Sequence Number1
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