MAUDE Adverse Event Report: ENCORE MEDICAL L.P HIP, STEM, CLP, STANDARD, SIZE#8, IMPLANT, POLISHED NECK; PROSTHESIS, HIP, HEMI-, FEMORAL, METAL/POLYMER, CEMENTED OR UNCEMENTED

Catalog Number 426-10-080

Device Problems Unstable (1667); Adverse Event Without Identified Device or Use Problem (2993)

Patient Problem Joint Laxity (4526)

Event Date 02/14/2024

Event Type  Injury  

Manufacturer Narrative

Complaint has been evaluated and is similar to previous report number 1644408-2018-00208; 426-10-030, s814 - stability, poor joint, revision surgery.If additional information regarding the reported event is submitted at a future date, this investigation will be re-evaluated.

Event Description

Revision surgery - due to instability.

• Brand Name: HIP, STEM, CLP, STANDARD, SIZE#8, IMPLANT, POLISHED NECK
• Type of Device: PROSTHESIS, HIP, HEMI-, FEMORAL, METAL/POLYMER, CEMENTED OR UNCEMENTED
• Manufacturer (Section D): ENCORE MEDICAL L.P; 9800 metric blvd; austin TX 78758
• Manufacturer (Section G): ENCORE MEDICAL L.P; 9800 metric blvd; austin TX 78758
• Manufacturer Contact: james mcmahon ; 9800 metric blvd; austin, TX 78758
• MDR Report Key: 18862565
• MDR Text Key: 337181549
• Report Number: 1644408-2024-00273
• Device Sequence Number: 1
• Product Code: KWY
• UDI-Device Identifier: 00888912079563
• UDI-Public: 00888912079563
• Combination Product (y/n): N
• Reporter Country Code: US
• PMA/PMN Number: K932481
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: Company Representative
• Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial
• Report Date: 03/07/2024

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?: No
• Device Operator: Health Professional
• Device Catalogue Number: 426-10-080
• Device Lot Number: 408N1042
• Was Device Available for Evaluation?: No
• Initial Date Manufacturer Received: 02/14/2024
• Initial Date FDA Received: 03/07/2024
• Was Device Evaluated by Manufacturer?: No
• Date Device Manufactured: 12/21/2021
• Is the Device Single Use?: Yes
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Initial
• Patient Sequence Number: 1
• Treatment: 00-03-321 LOT: 860B1215; 942-01-36F LOT: 622Z1031
• Patient Outcome(s): Required Intervention
• Patient Age: 69 YR
• Patient Sex: Female