MAUDE Adverse Event Report: ZM-930PA; TELEMETRY TRANSMITTER

Device Problem Overheating of Device (1437)

Patient Problem No Known Impact Or Consequence To Patient (2692)

Event Type  malfunction  

Event Description

(b)(4).

Manufacturer Narrative

The biomed at the hospital did not have the batteries used when the event occurred.They could not reproduce issue with the new batteries, advised (b)(6) to have the transmitter sent in for evaluation.They opted to continue using the transmitter on the floor.This historical complaint is being filed as part of a retrospective review of complaint files in response to a recent fda inspection.There is no change to the actual performance of any product and this report only represents an enhancement to the reporting criteria going forward.

• Brand Name: ZM-930PA
• Type of Device: TELEMETRY TRANSMITTER
• Manufacturer Contact: 1-31-4 nishiochia; shinjuku-ku, tokyo 161-8-560 ; 7050350
• MDR Report Key: 4385865
• MDR Text Key: 5262311
• Report Number: 8030229-2014-00126
• Device Sequence Number: 1
• Product Code: DRG
• Combination Product (y/n): N
• PMA/PMN Number: K946175
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: User Facility
• Type of Report: Initial

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 12/24/2014
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: No
• Device Operator: Other
• Date Manufacturer Received: 05/06/2013
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Date Device Manufactured: 10/01/2010
• Is the Device Single Use?: No
• Type of Device Usage: Reuse
• Patient Sequence Number: 1