MAUDE Adverse Event Report: MCKESSON MEDICAL SURGICAL, INC; SAFETY SYRINGE WITH NEEDLE

Catalog Number UNKNOWN

Device Problems Leak/Splash (1354); Detachment of Device or Device Component (2907)

Patient Problem Insufficient Information (4580)

Event Date 10/21/2021

Event Type  malfunction  

Event Description

The customer stated during administering the dosage while pushing down on the plunger it detached in the front of the needle and sprayed back from the end.No information was received regarding any serious injury as a result of this product malfunction.This complaint was initially reported to pfizer and pfizer forwarded to mckesson.

Manufacturer Narrative

Mckesson medical surgical is the assembler of a convenience kit on behalf of the sns that includes this safety syringe.The customer did not provide any product identification.We have notified asprsnsopscell@cdc.Gov and barda-rqaproductacceptance@hhs.Gov for awareness.

• Type of Device: SAFETY SYRINGE WITH NEEDLE
• Manufacturer (Section G): MCKESSON MEDICAL SURGICAL, INC; 1125 sycamore road; manteno IL 60950
• Manufacturer Contact: jo silverthorne ; 9954 mayland drive; richmond, VA 23233 ; 8045532278
• MDR Report Key: 12786450
• MDR Text Key: 281540961
• Report Number: 3017368639-2021-00184
• Device Sequence Number: 1
• Product Code: MEG
• Combination Product (y/n): N
• Reporter Country Code: US
• PMA/PMN Number: UNKNOWN
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: Other
• Reporter Occupation: Other
• Type of Report: Initial
• Report Date: 11/09/2021

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 11/10/2021
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Operator: Health Professional
• Device Catalogue Number: UNKNOWN
• Device Lot Number: UNKNOWN
• Was Device Available for Evaluation?: No
• Date Manufacturer Received: 10/21/2021
• Was Device Evaluated by Manufacturer?: No
• Is the Device Single Use?: Yes
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Initial
• Patient Sequence Number: 1
• Patient Outcome(s): Other