Enpath Medical, Inc. AngioDynamics Incorporated 21 Gauge Micro Access Needle, B-Bevel - 4 cm length, catalog No. 06506803 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
AngioDynamics Incorporated 21 Gauge Micro Access Needle, B-Bevel - 4 cm length, catalog No. 06506803
Brand
Enpath Medical, Inc.
Lot Codes / Batch Numbers
Lot W24005, Use By 2005-03
Products Sold
Lot W24005, Use By 2005-03
Enpath Medical, Inc. is recalling AngioDynamics Incorporated 21 Gauge Micro Access Needle, B-Bevel - 4 cm length, catalog No. 06506803 due to The product is labeled as sterile product but had not been sterilized.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The product is labeled as sterile product but had not been sterilized.
Recommended Action
Per FDA guidance
The only direct consignee, to whom the product was shipped, was notified of the recall by telephone and fax on February 26, 2004. The consignee was requested to the return the product and to sub-recall the product from their customers.
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, NY
Page updated: Jan 10, 2026