Arrow International Inc: Medical Device Recall in 2018 - (Recall #: Z-2576-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

Percutaneous Sheath Introducer Kit for use with 7 - 7.5 Fr. Catheters (8 Fr. 10 cm sheath length .035 inch dia. spring-wire guide), REF ES-09807. The percutaneous sheath introducer permits venous access and catheter introduction to the central circulation.

Product Classification:

Class II

Date Initiated: May 23, 2018

Date Posted: August 8, 2018

Recall Number: Z-2576-2018

Event ID: 80378

Reason for Recall:

Product contains dry natural rubber latex. Label states Latex Free.

Status: Terminated

Product Quantity: 60 units

Code Information:

Lot/Batch Number: 13F18A0037 Expiration Date/Expected Life: Apr 2019

Distribution Pattern:

Puerto Rico

Voluntary or Mandated:

Voluntary: Firm initiated