MAUDE Adverse Event Report: BECTON DICKINSON BD LANCET ULTRAFINE 33G GRAM(S); SINGLE USE ONLY BLOOD LANCET WITH AN INTEGRAL SHARPS INJURY PREVENTION FEATURE

Device Problem Adverse Event Without Identified Device or Use Problem (2993)

Patient Problem Insufficient Information (4580)

Event Type  Injury  

Event Description

This patient is pregnant.Other serious medical or important medical events.

• Brand Name: BD LANCET ULTRAFINE 33G GRAM(S)
• Type of Device: SINGLE USE ONLY BLOOD LANCET WITH AN INTEGRAL SHARPS INJURY PREVENTION FEATURE
• Manufacturer (Section D): BECTON DICKINSON
• MDR Report Key: 14397367
• MDR Text Key: 291713088
• Report Number: MW5109670
• Device Sequence Number: 1
• Product Code: FMK
• Combination Product (y/n): N
• Reporter Country Code: US
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Voluntary
• Reporter Occupation: Unknown
• Type of Report: Initial
• Report Date: 05/10/2022

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 05/12/2022
• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Patient Sequence Number: 1
• Patient Outcome(s): Other
• Patient Sex: Female