Arrow International Inc: Medical Device Recall in 2018 - (Recall #: Z-1299-2018)

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:

Pneumothorax Kit

Product Classification:

Class II

Date Initiated: October 24, 2017

Date Posted: April 11, 2018

Recall Number: Z-1299-2018

Event ID: 79294

Reason for Recall:

Product packaging may not be completely sealed.

Status: Terminated

Product Quantity: N/A

Code Information:

AK 01500 CA 01500

Distribution Pattern:

Nationally

Voluntary or Mandated:

Voluntary: Firm initiated