MAUDE Adverse Event Report: DEPUY ORTHOPAEDICS INC US CANCELLOUS BONE SCREW 6.5X25MM; BONE SCREWS AND PINS : SCREWS

Model Number	1172-25-000
Medical Device Problem Codes	Unintended Movement (3026); Migration (4003)
Health Effect - Clinical Codes	Pain (1994); No Code Available (3191)
Date of Event	06/22/2020
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
(b)(4).If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.
Event or Problem Description
The primary surgery was performed on (b)(6) 2002 via tha for the patient¿s right hip joint.It was reported that the revision surgery was performed on (b)(6) 2020 by replacing the cup (p/n: 124552000), the liner (p/n: 124012000), and the head (p/n: 853824) due to acetabular side¿s pain and migration.A stem (p/n: unknown) was remained because there was no remark of degeneration.The surgery was completed without any surgical delay.The surgeon thought that one of the factors was insufficiency of reaming for the cup.No further information is available.
Additional Manufacturer Narrative
Product complaint # (b)(4).Investigation summary: no device associated with this report was received for examination.A worldwide complaint database search found no other reported incident(s) against the provided product/lot combination(s) since release for distribution.Based on previous investigations this complication of joint replacement is unlikely to have been the result of a device failing to meet required specifications.The information received will be retained for potential series investigations if triggered by trend analysis, post market surveillance, or other events within the quality system.Corrective action was not indicated.H10 additional narrative: corrected: h6 (device).

• Brand Name: CANCELLOUS BONE SCREW 6.5X25MM
• Common Device Name: BONE SCREWS AND PINS : SCREWS
• Manufacturer (Section D): DEPUY ORTHOPAEDICS INC US; 700 orthopaedic drive; warsaw IN 46581 0988
• MDR Report Key: 10224339
• Report Number: 1818910-2020-14928
• Device Sequence Number: 19474256
• Product Code: HWC
• UDI-Device Identifier: 10603295007616
• UDI-Public: 10603295007616
• Combination Product (Y/N): N
• Initial Reporter Country: JA
• PMA/510(K) Number: K970929
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2002
• Device Explanted Year: 2020
• Reporter Type: Manufacturer
• Report Source: company representative,foreig
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 06/21/2020

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 Number: 1172-25-000
• Device Catalogue Number: 117225000
• Device Lot Number: WR3B14049
• Was Device Available for Evaluation?: No
• Initial Date Received by Manufacturer: 06/21/2020
• Supplement Date Received by Manufacturer: 07/24/2020
• Initial Report FDA Received Date: 07/02/2020
• Supplement Report FDA Received Date: 07/27/2020
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Concomitant Medical Products and Therapy/Usage Dates: CANCELLOUS BONE SCREW 6.5X25MM; CANCELLOUS BONE SCREW 6.5X25MM; CANCELLOUS BONE SCREW 6.5X35MM; DURALOC 1200 SERIES 52MM OD; ENDURON LINER NEUT 26ID X 52OD; P.F.C.* 26MM HEAD +5 MM; CANCELLOUS BONE SCREW 6.5X25MM; CANCELLOUS BONE SCREW 6.5X25MM; CANCELLOUS BONE SCREW 6.5X35MM; DURALOC 1200 SERIES 52MM OD; ENDURON LINER NEUT 26ID X 52OD; P.F.C.* 26MM HEAD +5 MM
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Age: 66 YR