Arrow International Inc: Medical Device Recall in 2016 - (Recall #: Z-2774-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

Catheter, Intravascular, Therapeutic, Short-Term Less than 30 days The Arrow CVC is indicated to provide short-term (<30 days) central venous access for treatment of diseases or conditions requiring central venous access.

Product Classification:

Class II

Date Initiated: February 17, 2016

Date Posted: September 21, 2016

Recall Number: Z-2774-2016

Event ID: 74898

Reason for Recall:

Notification of component molding abnormality by supplier used to package certain Arrow Select Kit (ASK) products.

Status: Terminated

Product Quantity: 6,121 units in total

Code Information:

Lot/Batch Numbers: 23F15L0662,23F15J0260,23F15K0983,23F15G0159,23F15J1102,23F15J0259 23F15C1225,23S15G0973,23F15H1033,23F15F0358,23F15K0345,23F15D1514 23F15C1226,23F15H0919,23F15E1091,23F15H0014,23F15D0241,23F15J0533 23F15E1094,23F15H0020,23F15H0740,23F15K1009,23F15J0431,23F15F1836 23F15H0857,23F15K0012,23F15M0313,23F15G0871,23F15J0285

Distribution Pattern:

US Distribution to states of: NC, OH, FL, and MD.

Voluntary or Mandated:

Voluntary: Firm initiated