FDADecember 28, 2023device

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.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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

What to do

FDA enforcement status: Ongoing

Brands named

mrp llc dba aquabilitimrpmrp llc

UPCs

1085980900501310859809005037

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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