| Brand Name | NA |
| Common Device Name | Stopcock, i.V. Set |
| Manufacturer (Section D) |
| BAXTER HEALTHCARE CORPORATION |
| deerfield IL |
|
| Manufacturer (Section G) |
| BAXTER HEALTHCARE - HAINA |
| parque industrial itabo |
| carretera sanchez km 18 1/2 |
| haina NA 21426 |
|
DR
21426
|
|
| Manufacturer Contact |
|
|
| 25212 w. illinois route 120 |
| round lake, IL 60073
|
|
+1(224)270-5355
|
|
| MDR Report Key | 50242041 |
| Report Number | 1416980-2026-02632 |
| Device Sequence Number | 9753085 |
| Product Code |
FMG
|
| UDI-Device Identifier | 00085412001913 |
| UDI-Public | (01)00085412001913 |
| Combination Product (Y/N) | N |
| Initial Reporter State | DC |
| Initial Reporter Country | US |
| PMA/510(K) Number | K130245 |
| Number of Events Summarized | 1 |
| Summary Report (Y/N) | N |
| Reporter Type |
Manufacturer
|
| Report Source |
Company Representative |
| Type of Report
| Initial,Followup |
| Report Date (Section B) |
09/14/2026 |
| 1 Device was Involved in the Event |
|
| 1 Patient was Involved in the Event |
|
| Is this an Adverse Event Report? |
No
|
| Is this a Product Problem Report? |
Yes
|
| Operator of Device |
Health Professional
|
| Device Model Number | 2C6204 |
| Device Catalogue Number | 2C6204 |
| Was Device Available for Evaluation? |
Yes
|
| Date Returned to Manufacturer | 07/23/2026 |
| Is the Reporter a Health Professional? |
No
|
| Type of Report(Section G) | Thirty-Day |
| Initial Date Received by Manufacturer | 07/15/2026 |
| Supplement Date Received by Manufacturer | 09/04/2026
|
| Initial Report FDA Received Date | 08/13/2026 |
| Supplement Report FDA Received Date | 09/14/2026
|
| Was Device Evaluated by Manufacturer? (Y/N) |
Yes
|
| Is the Device Labeled for Single Use? (Y/N) |
Yes
|
Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N) |
No
|
| Usage of Device |
Initial
|
| Patient Sequence Number | 1 |
| Patient Sex | Unknown |
|
|