Arrow International Inc: Medical Device Recall in 2019 - (Recall #: Z-1118-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

Arrow¿ Two-Lumen Central Venous Catheterization Kit with Blue FlexTip¿ Catheter Product Code: AH-11802 (OUS) GTN: 00801902026132

Product Classification:

Class II

Date Initiated: January 10, 2019

Date Posted: April 17, 2019

Recall Number: Z-1118-2019

Event ID: 82070

Reason for Recall:

The product lidstock contains a labelling error. The lidstock states the incorrect priming volume. The priming volumes printed on the extension lines are correct

Status: Terminated

Product Quantity: None (US)

Code Information:

Lot Numbers: 71F14E0696 71F14K0658 71F15E0493 71F15L0621 71F14E1541 71F14K1683 71F15F0090 71F15M0787 71F14F1154 71F14L0719 71F15H0574 71F16A0278 71F14H0474 71F14M1375 71F15H1503 71F16B0054 71F14H1215 71F15A0025 71F15J0570 71F16B1306 71F14J0852 71F15A1592 71F15J2098 71F14J1889 71F15D1460 71F15L0153

Distribution Pattern:

FL, NC

Voluntary or Mandated:

Voluntary: Firm initiated