Arrow International Inc: Medical Device Recall in 2017 - (Recall #: Z-2338-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

Arrow Pressure Injectable PICC Kit Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days The Arrow Pressure Injectable PICC is intended for short-term or long-term peripheral access to the central venous system for intravenous therapy and blood sampling.

Product Classification:

Class II

Date Initiated: May 9, 2017

Date Posted: June 21, 2017

Recall Number: Z-2338-2017

Event ID: 77232

Reason for Recall:

The Arrow Pressure Injectable PICC is intended for short-term or long-term peripheral access to the central venous system for intravenous therapy and blood sampling.

Status: Terminated

Product Quantity: 27,485 units distributed in U.S., 4,371 units distributed internationally

Code Information:

Material number: EU-04041-HPMSB, EU-05052-HPMSB, EU-05041-HPMSB Device Listing D000801

Distribution Pattern:

Worldwide Distribution - US (nationwide) and Canada

Voluntary or Mandated:

Voluntary: Firm initiated