FDA Adverse Event
Malfunction
Summary report: N
INSULIN SYRINGES WITH THE BD ULTRA-FINE NEEDLE, 1ML, 8MM, 31G
MDR report key: 1861375
·
Received October 4, 2010
Report
- Report Number
- MW5017690
- Event Type
- Malfunction
- Date Received
- October 4, 2010
- Date of Event
- September 14, 2010
- Report Date
- October 4, 2010
- Manufacturer
- BD
- Product Code
- FMI
- Product Problem
- Yes
- Report Source
- Voluntary report
- Reporter Location
- HI, US
- Reporter Occupation
- PHARMACIST
Narratives
Description of Event or Problem · 1
PHARMACY EMPLOYEE WAS PACKAGING A MAIL ORDER PRESCRIPTION WHICH INCLUDED INSULIN SYRINGES AND RECEIVED A NEEDLE STICK WHILE ATTEMPTING TO BUBBLE WRAP THE PRODUCT. IT WAS DETERMINED THAT TWO -2- OF THE TEN -10- SYRINGES DID NOT HAVE THE PROTECTIVE CAP ON THE NEEDLE. BD INSULIN SYRINGE WITH ULTRA FINE NEEDLE, 8 MM, 31 GAUGE, 1 ML NDC# 08290-8418-01 LOT # 01725145. DATES OF USE: (B)(6)2010.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | INSULIN SYRINGES WITH THE BD ULTRA-FINE NEEDLE, 1ML, 8MM, 31G | INSULIN SYRINGE | FMI | BD | 01725145 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |