MAUDE Adverse Event Report: ZIMMER BIOMET, INC. HYBRID GLENOID GLENOID BASE ARCOM; SHOULDER PROSTHESIS, SEMI-CONSTRAINED, METAL/POLYMER, UNCEMENTED / EXTREMITIES

Model Number 113952

Device Problems Device Dislodged or Dislocated (2923); Adverse Event Without Identified Device or Use Problem (2993); Loosening of Implant Not Related to Bone-Ingrowth (4002)

Patient Problems Pain (1994); Loss of Range of Motion (2032); Joint Dislocation (2374)

Event Date 08/06/2020

Event Type  Injury  

Manufacturer Narrative

(b)(4).Multiple mdr reports were filed for this event, please see associated reports: 0001825034-2022-01970; 0001825034-2022-01972; 0001825034-2022-01973; 0001825034-2022-01974.Concomitant medical products: item#: pt-113950, pt hybrid glen post regenerex; lot#: 607920; item#: 113611, comp primary stem 11mm micro, lot#: 821310; item#: 113032, versa-dial 42x18x46 hum head; lot#: 306460; item#: 118001, versa-dial/comp ti std taper; lot#: 926330.Customer has indicated that the product will not be returned to zimmer biomet for investigation, as the product location is unknown.The investigation is in process.Once the investigation has been completed, a follow-up mdr will be submitted.

Event Description

It was reported that the patient underwent a right shoulder arthroplasty.Subsequently, the patient had revision surgery approximately one (1) year and eight (8) months after the initial surgery due to pain, loss of range of motion, and loosening of the implants.

Manufacturer Narrative

This follow-up report is being submitted to relay additional information.No product was returned or pictures provided; visual and dimensional evaluations could not be performed.Medical records were not provided.Review of the device history record(s) identified no deviations or anomalies during manufacturing related to the reported event.A definitive root cause cannot be determined.If any further information which would change or alter any conclusions or information, a supplemental report will be filed accordingly.Zimmer biomet will continue to monitor for trends.

Event Description

No further event information available at the time of this report.

Manufacturer Narrative

(b)(4).This follow-up report is being submitted to relay additional and corrected information.Multiple mdr reports were filed for this event, please see associated reports: 0001825034-2022-01970-2, 0001825034-2022-01973-2.Once the investigation has been completed, a follow-up mdr will be submitted.

Event Description

It was reported that the patient underwent an anatomical right shoulder replacement approximately five (5) years and three (3) months ago.Subsequently, the patient underwent a revision surgery approximately three (3) years and seven (7) months ago due to pain and an insufficient rotator cuff.Prior to the surgery beginning, the patient's shoulder was easily dislocated anteriorly upon exam but stable posteriorly.The surgeon at that time decided to convert the patient's shoulder to a reverse due to an insufficient rotator cuff.The surgeon left the stem implant implanted, the surgery was completed without any complications.

• Brand Name: HYBRID GLENOID GLENOID BASE ARCOM
• Type of Device: SHOULDER PROSTHESIS, SEMI-CONSTRAINED, METAL/POLYMER, UNCEMENTED / EXTREMITIES
• Manufacturer (Section D): ZIMMER BIOMET, INC.; 56 e. bell drive; p.o. box 587; warsaw IN 46581
• Manufacturer (Section G): ZIMMER BIOMET, INC.; 56 e. bell drive; p.o. box 587; warsaw IN 46581
• Manufacturer Contact: jennifer rapsavage ; 56 e. bell dr.; warsaw, IN 46582 ; 5745260384
• MDR Report Key: 15310365
• MDR Text Key: 298773680
• Report Number: 0001825034-2022-01971
• Device Sequence Number: 1
• Product Code: MBF
• UDI-Device Identifier: 00880304462625
• UDI-Public: (01)00880304462625(17)230921(10)165380
• Combination Product (y/n): N
• Reporter Country Code: US
• PMA/PMN Number: K193038
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: Consumer,Health Professional
• Reporter Occupation: Physician
• Type of Report: Initial,Followup,Followup
• Report Date: 04/02/2024

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 08/29/2022
• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: Yes
• Device Operator: Health Professional
• Device Expiration Date: 09/21/2023
• Device Model Number: 113952
• Device Catalogue Number: 113952
• Device Lot Number: 165380
• Is the Reporter a Health Professional?: Yes
• Was the Report Sent to FDA?: No
• Date Manufacturer Received: 03/07/2024
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Date Device Manufactured: 09/21/2018
• 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
• Patient Outcome(s): Required Intervention; Hospitalization
• Patient Sex: Female