MAUDE Adverse Event Report: ZIMMER SURGICAL, INC. MEGMEET AC/DC ADAPTER (TYPE A); NONE AVAILABLE

Model Number N/A

Device Problem Material Frayed (1262)

Patient Problem No Patient Involvement (2645)

Event Date 09/23/2020

Event Type  malfunction  

Manufacturer Narrative

This event has been recorded by zimmer biomet under (b)(4).Once the investigation is complete, a follow up/final report will be submitted.

Event Description

It was reported that during routine testing the device was found with the cord ripped and with exposed wires.No adverse events were reported as a result of this malfunction.

Manufacturer Narrative

This event had been recorded by zimmer biomet under (b)(4).This medwatch is being filed to relay additional information.The following sections were updated/corrected: b4, b5, g3, g6, h2, h10.It has been determined that this device did not cause or contribute to a serious injury or a reportable malfunction.This mdr is a duplicate of 0001526350-2021-00024.The initial report was created in error and should be voided.

Event Description

It has been determined that this device did not cause or contribute to a serious injury or a reportable malfunction.This mdr is a duplicate of 0001526350-2021-00024.The initial report was created in error and should be voided.

• Brand Name: MEGMEET AC/DC ADAPTER (TYPE A)
• Type of Device: NONE AVAILABLE
• Manufacturer (Section D): ZIMMER SURGICAL, INC.; 200 west ohio avenue; dover OH 44622
• MDR Report Key: 11169489
• MDR Text Key: 228671853
• Report Number: 0001526350-2021-00045
• Device Sequence Number: 1
• Product Code: HAB
• Combination Product (y/n): N
• PMA/PMN Number: N/A
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: user facility
• Type of Report: Initial,Followup
• Report Date: 04/02/2021

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 01/14/2021
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Operator: Health Professional
• Device Model Number: N/A
• Device Catalogue Number: A301A000200
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 01/04/2021
• Was the Report Sent to FDA?: No
• Date Manufacturer Received: 04/01/2021
• Is This a Reprocessed and Reused Single-Use Device?: No
• Removal/Correction Number: N/A
• Patient Sequence Number: 1