MAUDE Adverse Event Report: ZIMMER BIOMET, INC. ZCA CUP 57X32 INCLINED SPACER; PROSTHESIS, HIP

Catalog Number 00800565432

Device Problem Device Dislodged or Dislocated (2923)

Patient Problems Bone Fracture(s) (1870); Joint Dislocation (2374); Muscle/Tendon Damage (4532); Unequal Limb Length (4534)

Event Date 06/30/2023

Event Type  Injury  

Event Description

It was reported a patient underwent a hip revision approximately two months¿ post implantation due to a dislocation.Attempts have been made and no further information is available.

Manufacturer Narrative

(b)(4).Multiple mdr reports were filed for this event, please see associated reports: 0001822565-2023-01974.G2: australia.D10: cat #: 802203202 / femoral head 12/14 taper 32 mm diameter +0 mm neck length / lot #: 3120473.The device will not be returned for analysis; however, an investigation of the reported event is in progress.Once the investigation is completed, a supplemental medwatch will be submitted.

Manufacturer Narrative

(b)(4).This follow-up report is being submitted to relay additional information.The following sections were updated/corrected.Updated: b4; b5; b7; d1; d2; d3; d4; g3; g4; h2; h3; h4.Correction: d6b - implant was not revised.D6b: device was not removed at during the revision procedure.Remains implanted.The investigation of the reported event is in progress.Once the investigation is completed, a supplemental medwatch will be submitted.

Event Description

It was reported a patient underwent a hip revision approximately two months¿ post implantation due to a dislocation.Attempts were made at closed reduction but were unsuccessful.It was then decided to complete an open reduction.The head was exchanged without any known complications.

Manufacturer Narrative

This follow-up report is being submitted to relay additional information.The reported event was confirmed by review of medical records.A healthcare professional reviewed the records and identified that the patient was reportedly sitting in bed when they went to turn, felt a pop in the hip, and had dislocated posteriorly with rotation found.Patient underwent an open reduction and head exchange.A small avulsion of the posterior greater trochanter was noted at the beginning of the procedure, as well as a ruptured fascial repair.No complications were noted post-op.Review of the device history records identified no deviations or anomalies during manufacturing.A definitive root cause could not be determined.If any further information is found which would change or alter any conclusions or information, a supplemental will be filed accordingly.Zimmer biomet will continue to monitor for trends.

Event Description

No additional information.

• Brand Name: ZCA CUP 57X32 INCLINED SPACER
• Type of Device: PROSTHESIS, HIP
• Manufacturer (Section D): ZIMMER BIOMET, INC.; 1800 w. center st.; warsaw IN 46580
• Manufacturer (Section G): ZIMMER BIOMET, INC.; 1800 w. center st.; warsaw IN 46580
• Manufacturer Contact: jennifer rapsavage ; 56 e. bell dr.; warsaw, IN 46582 ; 5745260384
• MDR Report Key: 17379456
• MDR Text Key: 319653191
• Report Number: 0001822565-2023-01975
• Device Sequence Number: 1
• Product Code: JDI
• UDI-Device Identifier: 00889024362819
• UDI-Public: (01)00889024362819(17)281207(10)64801070
• Combination Product (y/n): N
• Reporter Country Code: AS
• PMA/PMN Number: K191449
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: Foreign,Health Professional,Company Representative
• Reporter Occupation: Physician
• Type of Report: Initial,Followup,Followup
• Report Date: 08/22/2023

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
• Device Operator: Health Professional
• Device Catalogue Number: 00800565432
• Device Lot Number: 64801070
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Was the Report Sent to FDA?: No
• Initial Date Manufacturer Received: 06/30/2023
• Initial Date FDA Received: 07/24/2023
• Supplement Dates Manufacturer Received: 07/20/2023; 08/17/2023
• Supplement Dates FDA Received: 08/18/2023; 08/23/2023
• Was Device Evaluated by Manufacturer?: Yes
• Date Device Manufactured: 12/01/2020
• 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: SEE H10 NARRATIVE.
• Patient Outcome(s): Hospitalization; Required Intervention
• Patient Age: 62 YR
• Patient Sex: Female
• Patient Weight: 87 KG