Bard Peripheral Vascular Inc Recovery G2 Filter System - Jugular/Subclavian Delivery Kit, for use in the prevention of recurrent pulmonary embolism. Catalog Number RF-220J ***For Canada & Australia only*** Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Recovery G2 Filter System - Jugular/Subclavian Delivery Kit, for use in the prevention of recurrent pulmonary embolism. Catalog Number RF-220J ***For Canada & Australia only***
Brand
Bard Peripheral Vascular Inc
Lot Codes / Batch Numbers
Lot numbers: GFPK3279, GFPK3280, GFPK3281 & GFPK3282
Products Sold
Lot numbers: GFPK3279, GFPK3280, GFPK3281 & GFPK3282
Bard Peripheral Vascular Inc is recalling Recovery G2 Filter System - Jugular/Subclavian Delivery Kit, for use in the prevention of recurrent due to This action is being taken because BPV has recently received three complaints for the device that involve reports of introducer sheath tip damage. Th. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
This action is being taken because BPV has recently received three complaints for the device that involve reports of introducer sheath tip damage. The damage may result in loss of tip integrity.
Recommended Action
Per FDA guidance
Recall letters were sent to all consignees via Federal Express overnight delivery with signature receipt required on December 20, 2006. Each letter included a Recall and Effectiveness Check Form for each consignee to fill out and fax to Bard Peripheral Vascular, Inc (BPV). Customers will be asked to immediately remove product from inventory and isolated from use and contact BARD for return authorization. All returned product will be destroyed.
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