MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-06-14 for BD VACUTAINER? CPT? NH: ~130 IU FICOLL?: 2.0ML 362780 manufactured by Becton, Dickinson & Co..
[111635562]
Medical device lot #: 6061906, medical device expiration date: 03/31/2017, device manufacture date: 03/01/2016. (b)(6). Bd received samples and photos from the customer facility for investigation. The samples and photos were evaluated and the customer? S indicated failure mode with the incident lot was not observed. Additionally, a review of the manufacturing records was completed for the incident lot and no issues were identified.
Patient Sequence No: 1, Text Type: N, H10
[111635563]
It was reported that bd vacutainer? Cpt? Nh: ~130 iu ficoll? : 2. 0ml had poor barrier separation. No report of medical intervention or serious injury.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1917413-2018-02750 |
MDR Report Key | 7602739 |
Date Received | 2018-06-14 |
Date of Report | 2018-05-31 |
Date of Event | 2016-07-01 |
Date Mfgr Received | 2016-07-02 |
Device Manufacturer Date | 2015-07-31 |
Date Added to Maude | 2018-06-14 |
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? CPT? NH: ~130 IU FICOLL?: 2.0ML |
Generic Name | BLOOD SPECIMEN COLLECTION DEVICE |
Product Code | JCF |
Date Received | 2018-06-14 |
Catalog Number | 362780 |
Lot Number | 5212521 |
Device Expiration Date | 2016-08-31 |
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 | 2018-06-14 |