Arrow International Inc Arrow TheraCath Epidural Catheter - Product Usage: The Arrow Epidural Catheter permits access to the epidural space. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Arrow TheraCath Epidural Catheter - Product Usage: The Arrow Epidural Catheter permits access to the epidural space.
Brand
Arrow International Inc
Lot Codes / Batch Numbers
Product Code: EC-05000 Lot #: 13F18C0518
Products Sold
Product Code: EC-05000 Lot #: 13F18C0518
Arrow International Inc is recalling Arrow TheraCath Epidural Catheter - Product Usage: The Arrow Epidural Catheter permits access to the due to 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 . Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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.
Recommended Action
Per FDA guidance
Arrow sent a customer notification letter dated July 6, 2020. This letter informed customers of the affected product, asked them to check and remove inventory, and complete the response form.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026