MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a other,user facility report with the FDA on 2020-03-20 for BD VACUTAINER? SODIUM FLUORIDE POTASSIUM OXALATE (FX) BLOOD COLLECTION TUBES 367925 manufactured by Becton, Dickinson & Co. (broken Bow).
[186298681]
Device expiration date: unknown. Device manufacture date: unknown. A device evaluation is anticipated, but has not yet begun. Upon completion of the investigation, a supplemental report will be filed.
Patient Sequence No: 1, Text Type: N, H10
[186298682]
It was reported that overfill occurred after use with a bd vacutainer? Sodium fluoride potassium oxalate (fx) blood collection tubes. The following information was provided by the initial reporter, "the tube overfilled causing the study to be cancelled. Study was cancelled and pt has not returned for redraw. Customer doesn't feel the tube was over filled. It was the reference lab which rejected the specimen because too much plasma was submitted. They are used to getting plasma submitted from the 3-4 ml tubes not the 6 ml tube. Plasma was submitted for lactate testing. Site did not have lot# of tube. Spoke about there being a nominal fill indicator on tube label. Sent label brochure to customer to see the nominal fill line. "
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 1917413-2020-00304 |
| MDR Report Key | 9861401 |
| Report Source | OTHER,USER FACILITY |
| Date Received | 2020-03-20 |
| Date of Report | 2020-03-31 |
| Date of Event | 2020-02-29 |
| Date Mfgr Received | 2020-03-01 |
| Date Added to Maude | 2020-03-20 |
| Event Key | 0 |
| Report Source Code | Manufacturer report |
| Manufacturer Link | Y |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 3 |
| Reporter Occupation | OTHER HEALTH CARE PROFESSIONAL |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Manufacturer Contact | BDX BRETT WILKO |
| Manufacturer Street | 9450 SOUTH STATE STREET |
| Manufacturer City | SANDY UT 84070 |
| Manufacturer Country | US |
| Manufacturer Postal | 84070 |
| Manufacturer Phone | 8015652341 |
| Manufacturer G1 | BECTON, DICKINSON & CO. (BROKEN BOW) |
| Manufacturer Street | 150 SOUTH 1ST AVENUE |
| Manufacturer City | BROKEN BOW NE 68822 |
| Manufacturer Country | US |
| Manufacturer Postal Code | 68822 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | BD VACUTAINER? SODIUM FLUORIDE POTASSIUM OXALATE (FX) BLOOD COLLECTION TUBES |
| Generic Name | BLOOD SPECIMEN COLLECTION DEVICE |
| Product Code | JKA |
| Date Received | 2020-03-20 |
| Model Number | 367925 |
| Catalog Number | 367925 |
| Lot Number | UNKNOWN |
| Device Availability | * |
| Device Age | DA |
| Device Eval'ed by Mfgr | R |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | BECTON, DICKINSON & CO. (BROKEN BOW) |
| Manufacturer Address | 150 SOUTH 1ST AVENUE BROKEN BOW NE 68822 US 68822 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 2020-03-20 |