MAUDE Adverse Event Report: CATALYST ORTHOSCIENCE INC ARCHER R1 REVERSE SHOULDER SYSTEM; SHOULDER PROSTHESIS

Model Number	1230-7505-002
Medical Device Problem Code	Device Dislodged or Dislocated (2923)
Health Effect - Clinical Code	Failure of Implant (1924)
Date of Event	03/16/2022
Type of Reportable Event	Serious Injury
Event or Problem Description
It was reported that the patient was playing basketball and had his arm in extreme abduction when he felt a pop in his shoulder.The patient underwent revision surgery to remove and replace the humeral insert and humeral stem with another manufacturer's device approximately 05 months after the previous surgery.The humeral insert was found to be dissociated from the humeral stem.Customer has indicated that the implants will not be returned for investigation as the implants were discarded by the hospital.
Additional Manufacturer Narrative
Concomitant product: poly insert implant size 40 +4, 1230-7505-002, lot # 2105623.The revision surgery was completed as intended.The investigation is ongoing.Once the investigation has been completed, a follow-up mdr will be submitted.

• Brand Name: ARCHER R1 REVERSE SHOULDER SYSTEM
• Common Device Name: SHOULDER PROSTHESIS
• Manufacturer (Section D): CATALYST ORTHOSCIENCE INC; 14710 tamiami trail n.; suite 102; naples FL 34110
• Manufacturer Contact: dale davison ; 14710 tamiami trail n.; suite 102; naples, FL 34110 ; 2393259976
• MDR Report Key: 14074918
• Report Number: 3012552981-2022-00010
• Device Sequence Number: 20317947
• Product Code: PHX
• UDI-Device Identifier: 00811596030490
• UDI-Public: (01)00811596030490(17)260816(10)2105623
• Combination Product (Y/N): N
• Initial Reporter Country: US
• PMA/510(K) Number: K202611
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2021
• Device Explanted Year: 2022
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Health Professional
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial
• Report Date (Section B): 04/11/2022

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
• Operator of Device: Health Professional
• Device Expiration Date: 08/16/2026
• Device Model Number: 1230-7505-002
• Device Catalogue Number: 1230-7505-002
• Device Lot Number: 2105623
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 03/15/2022
• Initial Report FDA Received Date: 04/11/2022
• Was Device Evaluated by Manufacturer? (Y/N): Device Not Returned to Manufacturer
• Date Device Manufactured: 08/16/2021
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Concomitant Medical Products and Therapy/Usage Dates: 1230-7505-002, LOT # 2105623
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Sex: Male