Arrow International Inc ARROW EPIDURAL CATHETERIZATION KIT. Product No. MC-05001. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
ARROW EPIDURAL CATHETERIZATION KIT. Product No. MC-05001.
Brand
Arrow International Inc
Lot Codes / Batch Numbers
Lot No. RF4044686, expiration date 2006-09
Products Sold
Lot No. RF4044686, expiration date 2006-09
Arrow International Inc is recalling ARROW EPIDURAL CATHETERIZATION KIT. Product No. MC-05001. due to The recall is due to a confirmed packaging error of the wrong epidural needle (longer than stated).. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The recall is due to a confirmed packaging error of the wrong epidural needle (longer than stated).
Recommended Action
Per FDA guidance
The recalling firm sent a recall letter to its direct accounts to notify of the recall action and that the wrong epidural needle was packaged in the kits. The letter instructed the accounts to returned the kits to the recalling firm''s Asheboro, NC facility for rework and resterilization.
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 noticeDistribution
As reported by FDA
IN, TN, TX
Page updated: Jan 10, 2026