MAUDE Adverse Event Report: BECTON DICKINSON AND COMPANY BD CLEAR AND AMBER ENTERAL SYRINGES; TUBES, GASTROINTESTINAL (AND ACCESSORIES)

Device Problem Device Markings/Labelling Problem (2911)

Patient Problem Insufficient Information (4580)

Event Type  No Answer Provided  

Event Description

Potential error - it was noted by one of our pharmacists that we had bd clear and amber enteral syringes with no leading zeros on the measurement markings.(b)(6).Submission id: (b)(4).Circumstances or events have capacity to cause error.

• Brand Name: BD CLEAR AND AMBER ENTERAL SYRINGES
• Type of Device: TUBES, GASTROINTESTINAL (AND ACCESSORIES)
• Manufacturer (Section D): BECTON DICKINSON AND COMPANY
• MDR Report Key: 12598325
• MDR Text Key: 276112687
• Report Number: MW5104478
• Device Sequence Number: 1
• Product Code: KNT
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Voluntary
• Type of Report: Initial
• Report Date: 11/04/2020

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 10/07/2021
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: No
• Device Operator: No Information
• Was Device Evaluated by Manufacturer?: No Information
• Type of Device Usage: N
• Patient Sequence Number: 1