Arrow International Inc: Medical Device Recall in 2020 - (Recall #: Z-2801-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

Arrow Single Shot Epidural Anesthesia Kit - Product Usage: The Arrow Blunt Needle Single Shot Epidural Kit permits access to the epidural space.

Product Classification:

Class II

Date Initiated: July 6, 2020

Date Posted: August 19, 2020

Recall Number: Z-2801-2020

Event ID: 86044

Reason for Recall:

The lidstock states the incorrect expiration date for the product. This issue could result in use of a device that is expired which could potentially lead to an increased risk of infection or other complications. Sterility, biocompatibility, safety, or efficacy of the kits and their components are not assured beyond the correct expiration date.

Status: Terminated

Product Quantity: N/A

Code Information:

Product Code: AK-03000-S Lot #: 13F17J0230

Distribution Pattern:

World wide distribution

Voluntary or Mandated:

Voluntary: Firm initiated