FDA Adverse Event Malfunction Summary report: N

HYDROMID

MDR report key: 15474019 · Received September 23, 2022

Report

Report Number
3015060232-2022-00003
Event Type
Malfunction
Date Received
September 23, 2022
Date of Event
August 23, 2022
Report Date
August 23, 2022
Manufacturer
ACCESS VASCULAR INC.
Product Code
FOZ
UDI-DI
00850030354020
PMA / PMN Number
K203069
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
TX, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

(B)(6) (RN AT (B)(6) HEALTHCARE) REPORTED TO AVI TWO CASES OF SUSPECTED DVT ON THE SAME DAY USING THE SAME LOT OF PRODUCT. AS A RESULT, AVI IS SUBMITTING TWO MDRS. (THIS MDR) IS BEING REPORTED FOR SUSPECTED DVT FOR A MALE PATIENT POST-MIDLINE PLACEMENT. A MIDLINE HAD BEEN INSERTED IN THE PATIENT'S LEFT UPPER ARM ON (B)(6) 2022 AT AN INPATIENT FACILITY AND REQUIRED REMOVAL ON THE SAME DAY. (B)(6) WAS NOT ABLE TO VIEW THE ULTRASOUND REPORT AND THEREFORE WAS NOT ABLE TO CONFIRM SUSPICION OF DVT. (B)(6) NOTED THAT HE HAD TRIED DIFFERENT METHODS FOR HYDRATION, RATHER THAN FOLLOW THE PROVIDED IFU. (B)(6) (RN, AVI CLINICAL FIELD DIRECTOR) REINFORCED THE IMPORTANCE OF UTILIZING THE CORRECT METHOD FOR HYDRATION. THE LOT HISTORY RECORDS FOR THE FOLLOWING LOTS WERE REVIEWED AND DID NOT REVEAL ANY ANOMALIES OR DEVIATIONS THAT COULD HAVE CONTRIBUTED TO THE COMPLAINT ISSUE: 10122101, 11042102, 12092103, 11162103, 12162105, 11242103.

Description of Event or Problem · 0

SUSPECTED DEEP VEIN THROMBOSIS (DVT) POST MIDLINE PLACEMENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2827588 HYDROMID CATHETER, INTRAVASCULAR, THERAPEUTIC, SHORT-TERM LESS THAN 30 DAYS FOZ ACCESS VASCULAR INC. MID-141 11432076 00850030354020

Patients

Seq Age Sex Outcome Treatment
1 Male Other