MAUDE Adverse Event Report: DEVILBISS HEALTHCARE LLC DEVILBISS; SUCTION UNIT

Model Number 7325P-D

Device Problem Suction Failure (4039)

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

Event Date 08/26/2022

Event Type  malfunction  

Event Description

Devilbiss healthcare was notified of an incident involving a suction unit by a provider, who reported that the unit "quit suctioning, and the battery light is on, however, there is no suctioning and no sounds." there was no report or evidence of illness, injury or medical treatment associated with the complaint.The unit was discarded and could not be evaluated.

• Brand Name: DEVILBISS
• Type of Device: SUCTION UNIT
• Manufacturer (Section D): DEVILBISS HEALTHCARE LLC; 100 devilbiss drive; somerset PA 15501
• Manufacturer (Section G): DEVILBISS HEALTHCARE LLC; 100 devilbiss drive; somerset PA 15501
• Manufacturer Contact: jillian forster ; 99 seaview blvd; ste 210; port washington, NY 11050 ; 5169984600
• MDR Report Key: 15445787
• MDR Text Key: 304806757
• Report Number: 2515872-2022-00218
• Device Sequence Number: 1
• Product Code: JCX
• UDI-Device Identifier: 00885304032564
• UDI-Public: 00885304032564
• Combination Product (y/n): N
• Reporter Country Code: US
• PMA/PMN Number: K982304
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: Distributor
• Reporter Occupation: Other
• Remedial Action: Replace
• Type of Report: Initial
• Report Date: 09/19/2022

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 09/19/2022
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Model Number: 7325P-D
• Device Catalogue Number: 7325P-D
• Was Device Available for Evaluation?: No
• Date Manufacturer Received: 08/26/2022
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Date Device Manufactured: 06/21/2022
• Is the Device Single Use?: No
• Type of Device Usage: Unknown
• Patient Sequence Number: 1