FDA Adverse Event
Injury
Summary report: N
BECTON DICKINSON SAFETY GLIDE NEEDLE 25 GAUGE
MDR report key: 14934907
·
Received July 5, 2022
Report
- Report Number
- MW5110694
- Event Type
- Injury
- Date Received
- July 5, 2022
- Report Date
- July 1, 2022
- Manufacturer
- BD / BECTON DICKINSON
- Product Code
- FMI
- Product Problem
- Yes
- Report Source
- Voluntary report
- Reporter Location
- CA, US
- Reporter Occupation
- 501
- Health Professional
- Yes
Narratives
Description of Event or Problem · 0
BD SAFETYGLIDE NEEDLE 25G X 1 (MPN 305916), LOT # 2007149. WHEN THIS SPECIFIC LOT NUMBER IS CONNECTED TO A SYRINGE, THE PLUNGER IS VERY DIFFICULT TO COMPRESS. TESTED SEVERAL OTHER LOT NUMBERS FROM THE SAME PRODUCT AND HAD NO ISSUES. ISSUE ONLY APPEARS TO IMPACT LOT # 2007149. TEST DATE: (B)(6) 2022. ISSUE WAS IDENTIFIED AND TESTED IN OUR PEDIATRICS DEPARTMENT. DEPARTMENT CONTACT IS TIMOTHY WILLMAN. FDA SAFETY REPORT ID# (B)(4).
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 2765421 | BECTON DICKINSON SAFETY GLIDE NEEDLE 25 GAUGE | NEEDLE, HYPODERMIC, SINGLE LUMEN | FMI | BD / BECTON DICKINSON | 305916 | 2007149 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Unknown | Required Intervention |