MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-04-13 for BD VACUTAINER? SODIUM FLUORIDE 3.0MG N2E 6.0 MG PLUS BLOOD COLLECTION TUBES 367929 manufactured by Becton, Dickinson & Co..
[105672317]
Medical device expiration date: unknown. Device manufacture date: unknown. Investigation: bd had not received samples or photos from the customer facility for evaluation; therefore, the investigation was limited. Additionally, bd was unable to determine the specific lot number associated with this complaint. Therefore, a review of the device history record could not be conducted.
Patient Sequence No: 1, Text Type: N, H10
[105672318]
It was reported that there was foreign matter on the stopper of a bd vacutainer? Sodium fluoride 3. 0mg n2e 6. 0 mg plus blood collection tube before use. No injury or medical intervention.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1917413-2018-00792 |
MDR Report Key | 7427865 |
Date Received | 2018-04-13 |
Date of Report | 2018-04-12 |
Date of Event | 2017-01-27 |
Date Mfgr Received | 2017-01-27 |
Date Added to Maude | 2018-04-13 |
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 |
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 | 8015652845 |
Manufacturer G1 | BECTON, DICKINSON & CO. |
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 | 0 |
Brand Name | BD VACUTAINER? SODIUM FLUORIDE 3.0MG N2E 6.0 MG PLUS BLOOD COLLECTION TUBES |
Generic Name | BLOOD SPECIMEN COLLECTION DEVICE |
Product Code | OFZ |
Date Received | 2018-04-13 |
Catalog Number | 367929 |
Lot Number | UNKNOWN |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | BECTON, DICKINSON & CO. |
Manufacturer Address | 150 SOUTH 1ST AVENUE BROKEN BOW NE 68822 US 68822 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2018-04-13 |