FDA Adverse Event Malfunction Summary report: N

DPS HYPODERMIC SYRINGE LUER LOCK

MDR report key: 11998676 · Received June 14, 2021

Report

Report Number
MW5101869
Event Type
Malfunction
Date Received
June 14, 2021
Report Date
June 11, 2021
Manufacturer
DPS BARE / DUOPROSS MEDITECH CORPORATION
Product Code
MEG
Product Problem
Yes
Report Source
Voluntary report
Reporter Occupation
NURSE

Narratives

Description of Event or Problem · 1

[DPS BARE HYPODERMIC SYRINGE] USE FOR COVID-19 UNDER EMERGENCY USE AUTHORIZATION (EUA): STATE ANCILLARY SUPPLIES- DPS BARE HYPODERMIC SYRINGE, 1ML. LOT # 20110012, EXP DATE: 11-15-2025. SYRINGE BARREL HAS HUGE HOLE IN IT. FDA SAFETY REPORT ID# (B)(4).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
886405 DPS HYPODERMIC SYRINGE LUER LOCK SYRINGE, ANTISTICK MEG DPS BARE / DUOPROSS MEDITECH CORPORATION 2011012

Patients

Seq Age Sex Outcome Treatment
1