MAUDE Adverse Event Report: STRYKER INSTRUMENTS-A DIVISION OF STRYKER CORP MD SERIES LONG ANGLED ATTACHMENT; UNIT, OPERATIVE DENTAL

Model Number 5100015272

Device Problem Unintended Ejection (1234)

Patient Problem No Clinical Signs, Symptoms or Conditions (4582)

Event Date 09/30/2022

Event Type  malfunction  

Manufacturer Narrative

This record is a consolidation of records summarized as a part of the fda voluntary malfunction summary reporting program.Reported events: 1 event was reported for this quarter.Product return status: 1 device was not available for evaluation.Additional information: 1 device was not labeled for single-use.1 device was reprocessed or reused.

Event Description

This report summarizes 1 malfunction event in which the device reportedly unintentionally ejected the cutting device.1 event had patient involvement; no patient impact.

Manufacturer Narrative

Additional information: 1 device was not reprocessed or reused.

Event Description

This report summarizes 1 malfunction event in which the device reportedly unintentionally ejected the cutting device.1 event had patient involvement; no patient impact.

• Brand Name: MD SERIES LONG ANGLED ATTACHMENT
• Type of Device: UNIT, OPERATIVE DENTAL
• Manufacturer (Section D): STRYKER INSTRUMENTS-A DIVISION OF STRYKER CORP; 1941 stryker way; portage MI 49002
• Manufacturer (Section G): STRYKER INSTRUMENTS-KALAMAZOO; 4100 east milham avenue; kalamazoo MI 49001
• Manufacturer Contact: colette chung ; 1941 stryker way; portage, MI 49002 ; 2693237700
• MDR Report Key: 15663750
• MDR Text Key: 306707721
• Report Number: 3015967359-2022-02021
• Device Sequence Number: 1
• Product Code: EIA
• UDI-Device Identifier: 04546540391810
• UDI-Public: 04546540391810
• Combination Product (y/n): N
• Reporter Country Code: US
• Number of Events Reported: 1
• Summary Report (Y/N): Y
• Report Source: Manufacturer
• Source Type: Company Representative
• Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date: 01/30/2023

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Model Number: 5100015272
• Device Catalogue Number: 5100015272
• Device Lot Number: VMSR
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Initial Date Manufacturer Received: 09/30/2022
• Initial Date FDA Received: 10/24/2022
• Supplement Dates Manufacturer Received: 09/30/2022
• Supplement Dates FDA Received: 01/30/2023
• 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: Reuse
• Patient Sequence Number: 1