MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-02-13 for BD? SYRINGE 3ML HEPARIN 10 UNIT 306413 manufactured by Bd Medical (bd West) Medical Surgical.
[100065462]
Date of event: unknown. The date received by manufacturer has been used for this field. The customer's address is unknown. (b)(6), usa has been used as a default. A device evaluation is anticipated, but has not yet begun. Upon completion of the investigation and/or device history review, a supplemental report will be filed.
Patient Sequence No: 1, Text Type: N, H10
[100065463]
It was reported that multiple times, the plunger of a bd? Syringe 3ml heparin 10 unit will? Come out? While drawing up medication. There was no report of exposure, injury or medical intervention.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1911916-2018-00062 |
MDR Report Key | 7268220 |
Date Received | 2018-02-13 |
Date of Report | 2018-03-14 |
Date of Event | 2017-11-28 |
Date Mfgr Received | 2017-11-28 |
Device Manufacturer Date | 2017-04-21 |
Date Added to Maude | 2018-02-13 |
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 |
Reporter Occupation | PATIENT |
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 | BD MEDICAL (BD WEST) MEDICAL SURGICAL |
Manufacturer Street | 1852 10TH AVENUE |
Manufacturer City | COLUMBUS NE 68601 |
Manufacturer Country | US |
Manufacturer Postal Code | 68601 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 0 |
Brand Name | BD? SYRINGE 3ML HEPARIN 10 UNIT |
Generic Name | HEPARIN FLUSH |
Product Code | NZW |
Date Received | 2018-02-13 |
Catalog Number | 306413 |
Lot Number | 711169N |
Device Expiration Date | 2018-10-31 |
Operator | LAY USER/PATIENT |
Device Availability | * |
Device Age | DA |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | BD MEDICAL (BD WEST) MEDICAL SURGICAL |
Manufacturer Address | 1852 10TH AVENUE COLUMBUS NE 68601 US 68601 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2018-02-13 |