HEPARIN LOCK FLUSH, HEPARIN FLUSH

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-08-28 for HEPARIN LOCK FLUSH, HEPARIN FLUSH manufactured by Bd.

MAUDE Entry Details

• Report Number: MW5089436
• MDR Report Key: 8944875
• Date Received: 2019-08-28
• Date Added to Maude: 2019-08-29
• Event Key: 0
• Report Source Code: Voluntary report
• Manufacturer Link: N
• Number of Patients in Event: 0
• Adverse Event Flag: 3
• Product Problem Flag: 3
• Reprocessed and Reused Flag: 3
• Reporter Occupation: UNKNOWN
• Health Professional: 3
• Initial Report to FDA: 3
• Report to FDA: 3
• Event Location: 3
• Single Use: 3
• Previous Use Code: 3
• Event Type: 3
• Type of Report: 0

Device Sequence Number: 1

• Brand Name: HEPARIN LOCK FLUSH, HEPARIN FLUSH
• Generic Name: HEPARIN, VASCULAR ACCESS FLUSH
• Product Code: NZW
• Date Received: 2019-08-28
• Device Availability: *
• Device Eval'ed by Mfgr: *
• Device Sequence No: 1
• Device Event Key: 0
• Manufacturer: BD

Device Sequence Number: 2

• Brand Name: HEPARIN LOCK FLUSH, HEPARIN FLUSH
• Generic Name: HEPARIN, VASCULAR ACCESS FLUSH
• Product Code: NZW
• Date Received: 2019-08-28
• Device Availability: *
• Device Eval'ed by Mfgr: *
• Device Sequence No: 2
• Device Event Key: 0
• Manufacturer: BD

Patients

Patient Number	Treatment	Outcome	Date
1	0		2019-08-28