Arrow International Inc: Medical Device Recall in 2015 - (Recall #: Z-1080-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

ARROW Epidural Needle Component (product number AN-05501). Epidural needles permit access to the epidural space and are used as a conduit for epidural catheter placement.

Product Classification:

Class II

Date Initiated: January 5, 2015

Date Posted: February 18, 2015

Recall Number: Z-1080-2015

Event ID: 70177

Reason for Recall:

The product labeling does not specify the 5 year shelf life of the product.

Status: Terminated

Product Quantity: 63022

Code Information:

Product number AN-05501, Lot numbers: 23F13J0530, RF2108954, RF6127264, RF8045530, RF0021370, RF3014600, RF6127624, RF8070744, RF0035171, RF3026989, RF7031498, RF8083748, RF0050648, RF5084669, RF7043570, RF8096949, RF0075647, RF5094931, RF7088907, RF8123534, RF0092301, RF5106225, RF7090151, RF9015869, RF2021938, RF5118327, RF7102346, RF9030002, RF2044557, RF5120725, RF7113197, RF9071402, RF2058276, RF6081852, RF8018337, RF9098526, RF2083791, RF6092570, RF8020947, and RF9113319.

Distribution Pattern:

Distribution US Nationwide, Canada and Mexico.

Voluntary or Mandated:

Voluntary: Firm initiated