Arrow International Inc Peritoneal Lavage Kits, Model number AK-09000 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Peritoneal Lavage Kits, Model number AK-09000
Brand
Arrow International Inc
Lot Codes / Batch Numbers
Lot numbers: RF3111181 exp. 7/06, RF4012217 exp. 9/06, RF4012309 exp. 8/06, RF4012781 exp. 8/06, RF4023104 exp. 8/06, RF4034175 exp. 9/06, RF4034346 exp. 9/06, RF4034553 exp. 9/06, RF4055424 exp. 11/06, RF4055592 exp. 12/06, RF4055908 exp. 11/06, and RF4066874 exp. 12/06.
Products Sold
Lot numbers: RF3111181 exp. 7/06, RF4012217 exp. 9/06, RF4012309 exp. 8/06, RF4012781 exp. 8/06, RF4023104 exp. 8/06, RF4034175 exp. 9/06, RF4034346 exp. 9/06, RF4034553 exp. 9/06, RF4055424 exp. 11/06, RF4055592 exp. 12/06, RF4055908 exp. 11/06, and RF4066874 exp. 12/06.
Arrow International Inc is recalling Peritoneal Lavage Kits, Model number AK-09000 due to wrong introducer needle in some kits. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
wrong introducer needle in some kits
Recommended Action
Per FDA guidance
The recalling firm issued a recall letter to their customers on 8/9/04. The letter instructed the accounts to return the product.
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