MAUDE Adverse Event Report: ACUMED LLC ARH SLIDE-LOC¿ HEAD 22MM, RIGHT; PROSTHESIS, ELBOW, HEMI-, RADIAL, HEAD

Model Number 5001-0222R-S

Device Problem Unstable (1667)

Patient Problem No Code Available (3191)

Event Date 05/25/2017

Event Type  Injury  

Manufacturer Narrative

Additional mdrs associated with this event: 3025141-2017-00138: stem.3025141-2017-00139: neck.

Event Description

A patient has a arh slide-loc radial head replacement implanted.The patient continued to have an unstable elbow that required additional surgery.It was not known if the arh slide-loc implants were the source of the instability.During the additional surgery, it was determined that the arh slide-loc implants were intact and did not require removal or change.The implants were left in place in the patient's elbow.

• Brand Name: ARH SLIDE-LOC¿ HEAD 22MM, RIGHT
• Type of Device: PROSTHESIS, ELBOW, HEMI-, RADIAL, HEAD
• Manufacturer (Section D): ACUMED LLC; 5885 nw cornelius pass road; hillsboro OR 97124 9432
• Manufacturer (Section G): ACUMED LLC; 5885 nw cornelius pass road; hillsboro OR 97124 9432
• Manufacturer Contact: micki lehman ; 5885 nw cornelius pass road; hillsboro, OR 97124-9432 ; 8886279957
• MDR Report Key: 6659913
• MDR Text Key: 78160845
• Report Number: 3025141-2017-00137
• Device Sequence Number: 1
• Product Code: KWI
• Combination Product (y/n): N
• Reporter Country Code: US
• PMA/PMN Number: K131845
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: distributor
• Reporter Occupation: Other
• Type of Report: Initial
• Report Date: 05/30/2017

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 06/22/2017
• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Device Operator: Physician
• Device Expiration Date: 06/07/2023
• Device Model Number: 5001-0222R-S
• Device Catalogue Number: 5001-0222R-S
• Device Lot Number: 379587
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Date Manufacturer Received: 05/30/2017
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Date Device Manufactured: 06/17/2016
• 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 Age: 53 YR