MAUDE Adverse Event Report: BIOHORIZONS, INC. BIOHORIZONS ABUTMENT SCREW, MULTI-UNIT ABUTMENT; MULIT-UNIT ABUTMENT SCREW

Model Number PXMUAS

Device Problem Material Deformation (2976)

Patient Problem No Information (3190)

Event Type  malfunction  

Manufacturer Narrative

No evaluation performed for no product was returned for investigation.

Event Description

Stripped abutment screw.

• Brand Name: BIOHORIZONS ABUTMENT SCREW, MULTI-UNIT ABUTMENT
• Type of Device: MULIT-UNIT ABUTMENT SCREW
• Manufacturer (Section D): BIOHORIZONS, INC.; 2300 riverchase center; birmingham 35244
• Manufacturer (Section G): BIOHORIZONS, INC.; 2300 riverchase center; birmingham 35244
• Manufacturer Contact: anissa smith ; 2300 riverchase center; birmingham 35244 ; 2059867880
• MDR Report Key: 7895733
• MDR Text Key: 121567228
• Report Number: 1060818-2018-00084
• Device Sequence Number: 1
• Product Code: NHA
• Combination Product (y/n): N
• Reporter Country Code: US
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: company representative
• Reporter Occupation: Other Health Care Professional
• Type of Report: Initial
• Report Date: 09/20/2018

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 09/20/2018
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Operator: Health Professional
• Device Model Number: PXMUAS
• Device Lot Number: PO17013181
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Is the Device Single Use?: No
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Unknown
• Patient Sequence Number: 1