13 MM SS VIAL ACCESS DEVICE
Report
- Report Number
- 9616066-2024-01973
- Event Type
- Malfunction
- Date Received
- December 9, 2024
- Date of Event
- October 17, 2024
- Report Date
- January 5, 2025
- Manufacturer
- BECTON DICKINSON
- Product Code
- LHI
- UDI-DI
- 07613203011792
- PMA / PMN Number
- K233021
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- NE, US
- Reporter Occupation
- OTHER HEALTH CARE PROFESSIONAL
- Health Professional
- Yes
Narratives
DUE TO NO SAMPLE BEING RECEIVED, AN INVESTIGATION COULD NOT BE PERFORMED, AND A ROOT CAUSE COULD NOT BE DETERMINED. NO PRODUCT WILL BE RETURNED PER CUSTOMER. NO INVESTIGATION WAS PERFORMED.
INITIAL MDR SUBMISSION. A FOLLOW UP MDR WILL BE SUBMITTED IF ADDITIONAL INFORMATION, A DEVICE EVALUATION, OR A DEVICE HISTORY REVIEW IS COMPLETED.
MATERIAL#: 2203E. BATCH NUMBER#: 23105217. IT WAS REPORTED BY CUSTOMER THAT VIAL ADAPTOR LEAKING DURING USE VERBATIM#: RCC RECEIVED A COMPLAINT VIA EMAIL. COVE ID - (B)(4). DATE OF COMPANY AWARENESS- 17-OCT-24. MERCK FG BATCH # - Y008793. BD VIAL ADAPTER BATCH - 23105217. PQC CATEGORY - VIAL ADAPTOR LEAKING DURING USE.
MATERIAL#: 2203E. BATCH NUMBER#: 23105217. IT WAS REPORTED BY CUSTOMER THAT VIAL ADAPTOR LEAKING DURING USE. VERBATIM#: RCC RECEIVED A COMPLAINT VIA EMAIL. EMAIL(S) ATTACHED. COVE ID - (B)(4). DATE OF COMPANY AWARENESS- 17-OCT-2024. MERCK FG BATCH # - Y008793. BD VIAL ADAPTER BATCH - 23105217. PQC CATEGORY - VIAL ADAPTOR LEAKING DURING USE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 2477100 | 13 MM SS VIAL ACCESS DEVICE | SET, I.V. FLUID TRANSFER | LHI | BECTON DICKINSON | 23105217 | 07613203011792 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA | Unknown |