MAUDE Adverse Event Report: SHARPS CONTAINER; CONTAINER, SHARPS

Device Problem Output Problem (3005)

Patient Problem Insufficient Information (4580)

Event Type  Injury  

Event Description

Event: spoke "w pt and apos's" husband.Sharps container was left out of order.They did not receive one.

• Brand Name: SHARPS CONTAINER
• Type of Device: CONTAINER, SHARPS
• MDR Report Key: 13142405
• MDR Text Key: 283178430
• Report Number: MW5106419
• Device Sequence Number: 1
• Product Code: MMK
• Combination Product (y/n): N
• Reporter Country Code: US
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Voluntary
• Reporter Occupation: Other Health Care Professional
• Type of Report: Initial
• Report Date: 12/28/2021

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 12/30/2021
• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Patient Sequence Number: 1
• Treatment: HUMITA CF 40MG/0.4ML PEN (2=2); INJECT 1 PEN (40 MG TOTAL) UNDER THE SKIN EVERY 14 DAYS. ; LEXAPRO TAB 5MG; OTEZLA ; PANTOPRAZOLE INJ SOD 40MG; PREDNISONE TAB 10MG; SUCCINYLCHOL INJ 200/10ML
• Patient Sex: Female