FDA Adverse Event
Malfunction
Summary report: N
ACCESS WASH BUFFER II
MDR report key: 2252402
·
Received September 17, 2011
Report
- Report Number
- 2122870-2011-03774
- Event Type
- Malfunction
- Date Received
- September 17, 2011
- Date of Event
- August 17, 2011
- Report Date
- August 17, 2011
- Manufacturer
- BECKMAN COULTER INC.
- Product Code
- LDT
- PMA / PMN Number
- EXEMPT
- Removal / Correction Number
- N/A
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CH
- Reporter Occupation
- OTHER
Narratives
Additional Manufacturer Narrative · 1
NO CLEAR ROOT CAUSE COULD BE DETERMINED FOR THIS EVENT. (B)(4).
Additional Manufacturer Narrative · 1
(B)(4)
Description of Event or Problem · 1
REPLACEMENT WAS SENT TO THE CUSTOMER.
Description of Event or Problem · 1
A CUSTOMER CONTACTED BECKMAN COULTER INC. (BEC) TO REPORT RECEIVING ONE DXI WASH BUFFER II CUBETAINER THAT LEAKED. THE CUSTOMER DID NOT QUESTION ANY PATIENT RESULTS. NO INJURY OR AFFECT TO PATIENT OR END USER IN ASSOCIATION WITH THIS EVENT WAS REPORTED. VISUAL INSPECTION OF THE PHOTO IS INCONCLUSIVE AND DID NOT SUPPORT THE PIN HOLE LEAK AND/OR STRESS CRACK AS THE ROOT CAUSE OF THIS EVENT.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | ACCESS WASH BUFFER II | REAGENT, GENERAL PURPOSE | LDT | BECKMAN COULTER INC. | WASH BUFFER II | 331800F |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 |