Swabcap and Swabflush

• • Ongoing Z-2199-2025 FDA Class II ·initiated 16 Jun 2025

  SwabFlush syringes are affected by the ICU Medical recall of their SwabCap Disinfecting Cap due to a manufacturing issue which affects the seal between the foil lid and plastic container of the Swab Cap. The issue may result in a reduced level of disinfection of the luer access valve, potentially resulting in patient infection/sepsis.

• • Ongoing Z-2116-2025 FDA Class II ·initiated 3 Jun 2025

  Due to a manufacturing issue, disinfecting cap for needle-free connectors may have an incomplete seal between the foil lid and plastic container, which may result in isopropyl alcohol evaporation from the sponge, which may result in inadequate disinfection.

510(k) Number

K130975 ↗

FDA Product Code

QBP

Device Class

Class II

Regulation

21 CFR Part 880.5440

Advisory Committee

General Hospital

FDA Decision

SESE Substantially Equivalent

• Microbore Extension Set

  Class II

  FDA 510(k) K942349 Active Cleared 8 Feb 1995

• 0.9% Sodium Chloride Injection, USP - 2.5 mL in 3 mL Syringe, 0.9% Sodium Chloride Injection, USP-3mL in 10 mL Syringe, 0.9% Sodium Chloride Injection, USP - 5 mL in 10 mL Syringe, 0.9% Sodium Chloride Injection, USP - 10 mL in 10 mL Syringe

  Class II

  FDA 510(k) K142620 Active Cleared 12 Dec 2014

• Swabcap

  Class II

  FDA 510(k) K083508 Active Cleared 28 Apr 2009

• Syrex Heparin Lock Flush Syringe, 1 Unit/Ml & 2 Units/Ml

  Class II

  FDA 510(k) K061497 Active Cleared 23 Feb 2007

• Syrex Pre-Filled Syringe

  Class II

  FDA 510(k) K023740 Active Cleared 13 May 2003

• Excelsior Disposable Syringe W/Normal Saline (.9% Sodium Chloride)

  Class II

  FDA 510(k) K962938 Active Cleared 25 Oct 1996

See all devices from Excelsior Medical LLC →