FDA Adverse Event Malfunction Summary report: N

RIGIDFIX MALLET *EA

MDR report key: 11784995 · Received May 6, 2021

Report

Report Number
1221934-2021-01427
Event Type
Malfunction
Date Received
May 6, 2021
Report Date
April 15, 2021
Manufacturer
DEPUY MITEK LLC US
Product Code
LXH
UDI-DI
10886705002993
PMA / PMN Number
EXEMPT
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
UK
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

UDI: (B)(4). INCOMPLETE. THE EXPIRATION DATE IS CURRENTLY UNAVAILABLE. INVESTIGATION SUMMARY: BACKGROUND: THE MALLET¿S HANDLE HAS COME OFF IN SURGEON¿S HANDS DURING THE PROCEDURE. INVESTIGATION SUMMARY: THE RIGIDFIX MALLET *EA (PART #: 213705, LOT #: UNK) WAS RECEIVED AND EVALUATED AT US CQ. UPON VISUAL INSPECTION, THE MALLET HANDLE BROKE OFF THE HEAD. THERE WERE SCRATCHES OBSERVED ON THE BOTH THE FACES OF THE MALLET HEAD. HENCE, THE REPORTED CONDITION CAN BE CONFIRMED. THE POSSIBLE ROOT CAUSE FOR THE REPORTED CONDITION CAN BE THAT THE DEVICE ENCOUNTERED UNINTENDED FORCES DURING ITS USE. DURING THE INVESTIGATION, NO PRODUCT DESIGN OR MANUFACTURING ISSUES WERE OBSERVED THAT MAY HAVE CONTRIBUTED TO THE COMPLAINT CONDITION. BASED ON THE INVESTIGATION FINDINGS, IT HAS BEEN DETERMINED THAT NO CORRECTIVE AND/OR PREVENTATIVE ACTION IS PROPOSED. HOWEVER, DEPUY SYNTHES MITEK WILL CONTINUE TO TRACK ANY RELATED COMPLAINTS WITHIN THIS DEVICE FAMILY AS A MEANS OF MONITORING THE EXTENT TO WHICH THIS COMPLAINT IS OBSERVED IN THE FIELD.

Description of Event or Problem · 1

IT WAS REPORTED BY THE SALES REP IN (B)(6) THAT DURING AN ARTHROPLASTY PROCEDURE ON AN UNKNOWN DATE, IT WAS OBSERVED THAT THE HANDLE ON THE RIGIDFIX MALLET DEVICE CAME OFF THE SURGEON'S HAND. ANOTHER LIKE DEVICE WAS USED TO COMPLETE THE PROCEDURE WITHOUT DELAY. THERE WERE NO ADVERSE PATIENT CONSEQUENCES REPORTED. NO ADDITIONAL INFORMATION WAS PROVIDED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
680502 RIGIDFIX MALLET *EA SURGICAL MALLET LXH DEPUY MITEK LLC US 213705 10886705002993

Patients

Seq Age Sex Outcome Treatment
1