MAUDE Adverse Event Report: FX SOLUTIONS HUMERIS REVERSED; REVERSE SHOULDER PROSTHESIS

Model Number UNIQUE SIZE

Device Problems Loose or Intermittent Connection (1371); Appropriate Term/Code Not Available (3191)

Patient Problem Insufficient Information (4580)

Event Date 03/29/2021

Event Type  Injury  

Manufacturer Narrative

The event took place outside of the united states ((b)(6)) and was associated with a product that is also cleared for the market within the united states.

Event Description

The event was a revision surgery due to loosening that occured approximately 2 months after the primary surgery.The primar surgery used the humeris reversed system.The surgeon explained the loosening of the baseplate was coming from a too high bone graft that made it unstable.The surgeon explanted the ø24 baseplate and the 10mm post extension and they were replaced by the same products.He explanted the ø36/+3 135/145 humeral cup and replaced it by a ø40/+3 135/145 humeral cup.He explanted also the ø36 centered glenosphere and replaced it by a ø40 centered glenosphere.He also explanted associated scews.

• Brand Name: HUMERIS REVERSED
• Type of Device: REVERSE SHOULDER PROSTHESIS
• Manufacturer (Section D): FX SOLUTIONS; 1663 rue des majornas; viriat, 01440 ; FR 01440
• Manufacturer (Section G): FX SOLUTIONS; 1663 rue des majornas; viriat, 01440 ; FR 01440
• Manufacturer Contact: ratsamy thevenin ; 1663 rue des majornas; viriat, 01440 ; FR 01440
• MDR Report Key: 11892142
• MDR Text Key: 252887321
• Report Number: 3009532798-2021-00060
• Device Sequence Number: 1
• Product Code: PHX
• UDI-Device Identifier: 03701037300237
• UDI-Public: 03701037300237
• Combination Product (y/n): N
• Reporter Country Code: FR
• PMA/PMN Number: K150488
• 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: 05/17/2021

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 Model Number: UNIQUE SIZE
• Device Catalogue Number: 105-0024
• Device Lot Number: P1305
• Was Device Available for Evaluation?: No
• Initial Date Manufacturer Received: 04/02/2021
• Initial Date FDA Received: 05/27/2021
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Date Device Manufactured: 01/20/2021
• 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
• Patient Outcome(s): Required Intervention