MAUDE Adverse Event Report: HILL-ROM MEXICO GS-300 GEN EXAM LT W/TABLE/WALL MT DOM; DEVICE, MEDICAL EXAMINATION, AC POWERED

Model Number 44410

Device Problem Fire (1245)

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

Event Date 08/25/2022

Event Type  malfunction  

Event Description

The customer reported that the base of the gs300 caught fire near the plug which then caused the gooseneck of the light to pop out of the base.There were no injuries caused by the reported event.This complaint was captured under hillrom ref # (b)(4).

Manufacturer Narrative

The welch allyn gs 300 is an exam light, designed to meet the various needs of the physician¿s office, hospital environment and specialist¿s office.It is not intended for rendering diagnosis or surgery.The gs 300 light is mounted on a mobile stand or table/wall mount.To prevent injury from exposed wires and damaged housing, there are warnings in the dfu including: inspect the device for wear, fraying, or other damage.Do not use if you see signs of damage, if the instrument malfunctions, appears not to be working properly, or if you notice a change in performance.If a device were to get hot to touch, spark, have burn marks or burned components a trained clinician would not use the device and remove it from the patient's environment.The customer has not returned the device, therefore, no further investigation into the root cause of the reported issue could be performed.Based on the picture provided this event has been likely caused by a short circuit inside the control box assembly.Although the reported event did not result in a serious injury to the customer or the patients, a report of a fire in a clinical environment could cause a serious injury if it had to recur.Therefore, hillrom consider this event reportable.Based on the information provided at this time no further action is required.

• Brand Name: GS-300 GEN EXAM LT W/TABLE/WALL MT DOM
• Type of Device: DEVICE, MEDICAL EXAMINATION, AC POWERED
• Manufacturer (Section D): HILL-ROM MEXICO; ave.del telefono no. 200 col.; apodaca, nuevo leon 66640 ; MX 66640
• Manufacturer Contact: antonio acquafredda ; 1069 state route 46 east; batesville, IN 47006 ; 8129310130
• MDR Report Key: 15418272
• MDR Text Key: 299870309
• Report Number: 3006087789-2022-00001
• Device Sequence Number: 1
• Product Code: KZF
• UDI-Device Identifier: 00732094073898
• UDI-Public: 732094073898
• Combination Product (y/n): N
• Reporter Country Code: US
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: User Facility
• Reporter Occupation: Other
• Type of Report: Initial
• Report Date: 09/14/2022

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 09/14/2022
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Model Number: 44410
• Device Lot Number: (10)1647
• Was Device Available for Evaluation?: No
• Was the Report Sent to FDA?: No
• Date Manufacturer Received: 08/25/2022
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Reuse
• Patient Sequence Number: 1