MAUDE Adverse Event Report: BARD ACCESS SYSTEMS HUBER PLUS 20G X 0.75" NEEDLELESS Y SITE; SET, ADMINISTRATION, INTRAVASCULAR

Model Number	N/A
Medical Device Problem Code	Fluid/Blood Leak (1250)
Health Effect - Clinical Code	No Patient Involvement (2645)
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
The device has not been returned to the manufacturer for evaluation.A lot history review (lhr) of reds1094 showed two other similar product complaint(s) from this lot number.
Event or Problem Description
On 08 june 2020: it was reported the y point of the griper is defective, which when purging it sells the liquid through the bioconnector of the y point.No other information was provided.

• Brand Name: HUBER PLUS 20G X 0.75" NEEDLELESS Y SITE
• Common Device Name: SET, ADMINISTRATION, INTRAVASCULAR
• Manufacturer (Section D): BARD ACCESS SYSTEMS; 605 n. 5600 w.; salt lake city UT 84116
• MDR Report Key: 10192955
• Report Number: 3006260740-2020-02228
• Device Sequence Number: 11000563
• Product Code: FPA
• UDI-Device Identifier: 00801741065637
• UDI-Public: (01)00801741065637
• Combination Product (Y/N): N
• Initial Reporter Country: SP
• PMA/510(K) Number: K993848
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: distributor
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial
• Report Date (Section B): 06/24/2020

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: Health Professional
• Device Model Number: N/A
• Device Catalogue Number: 012034NY
• Device Lot Number: REDS1094
• Was Device Available for Evaluation?: No
• Event Location: Hospital
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 06/05/2020
• Initial Report FDA Received Date: 06/24/2020
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1