FDA Enforcement Class II Ongoing

AQUABILITI AQUASTAT 0.9% Sodium Chloride Injection syringe, USP, 5mL in 12mL, REF 2T0805; and 3mL in 12mL, REF 2T0807, intermediate cartons containing 100 syringes, shipping cases containing 400 syringes, Rx, Sterile.

Recall: Z-1174-2024 · Reported February 28, 2024

Enforcement

Recall Number
Z-1174-2024
Event ID
93848
Classification
Class II
Status
Ongoing
Product Type
Devices
Firm
MRP, LLC dba Aquabiliti
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
February 28, 2024
Initiation Date
December 28, 2023
Classification Date
February 22, 2024
Address
5209 Linbar Dr Ste 640, N/A, Nashville, TN, 37211-1026, United States

Description

AQUABILITI AQUASTAT 0.9% Sodium Chloride Injection syringe, USP, 5mL in 12mL, REF 2T0805; and 3mL in 12mL, REF 2T0807, intermediate cartons containing 100 syringes, shipping cases containing 400 syringes, Rx, Sterile.

Reason

The saline flush syringes may fail to meet USP criteria for stated sodium chloride content after 12 months.

Code Info

REF 2T0805 - Lot numbers KH04910, exp. 1/11/2024; KH04930, exp. 3/13/2024; KH04954, exp. 5/22/2024; KH04975, exp. 8/2/2024; KH04990, exp. 9/6/2024; KH05020, exp. 10/23/2024; KH05022, exp. 10/24/2024; KH05043, exp. 11/13/2024; KH05066, exp. 12/13/2024; KH05068, exp. 12/14/2024; KH05070, exp. 12/18/2024; KH05073, exp. 12/20/2024; KH05134, exp. 6/25/2025; KH05135, exp. 6/27/2025; and KH05152, exp. 10/10/2025; UDI-DI 10859809005013. REF 2T0807 - Lot numbers KH04909, exp. 1/10/2024; KH04944, exp. 4/24/2024; KH04986, exp. 8/30/2024; KH04988, exp. 9/5/2024; KH05024, exp. 10/25/2024; KH05026, exp. 10/26/2024; and KH05071, exp. 12/19/2024; UDI-DI 10859809005037.

Distribution

US Nationwide distribution in the states CO, FL, NC, NY, OH, PA, TN, TX, and VA.

Quantity

3,080,000 syringes