C.R. Bard Access Systems, Inc Bard Access Systems, Inc., Ponsky* PEG (Percutaneous Endoscopic Gastrostomy) Safety System - "Pull", REF 006035, 20F, Sterile. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Bard Access Systems, Inc., Ponsky* PEG (Percutaneous Endoscopic Gastrostomy) Safety System - "Pull", REF 006035, 20F, Sterile.
Brand
C.R. Bard Access Systems, Inc
Lot Codes / Batch Numbers
Lots: 43ARA077, 43GQA067, 43HQA055, 43HQA168, 43JQA058, 43KQA074, 43LQA077, HURA1476, HURD1278, HURE2825, HURE3304, HURE3305, HURF0408, HURG1389, HURI0673, HURJ0011, HURJ0539, HURJ0540, HURJ0541, HURJ0542, HURJ0543, HURK0672, HURL0316, HUSA0278, HUSB0099, HUSC0160, HUSC2105, HUSD1941, HUSD1942, HUSE0936, HUSF0002, HUSF1751, HUSF1752.
Products Sold
Lots: 43ARA077, 43GQA067, 43HQA055, 43HQA168, 43JQA058, 43KQA074, 43LQA077, HURA1476, HURD1278, HURE2825, HURE3304, HURE3305, HURF0408, HURG1389, HURI0673, HURJ0011, HURJ0539, HURJ0540, HURJ0541, HURJ0542, HURJ0543, HURK0672, HURL0316, HUSA0278, HUSB0099, HUSC0160, HUSC2105, HUSD1941, HUSD1942, HUSE0936, HUSF0002, HUSF1751, HUSF1752.
C.R. Bard Access Systems, Inc is recalling Bard Access Systems, Inc., Ponsky* PEG (Percutaneous Endoscopic Gastrostomy) Safety System - "Pull", due to The Polypectomy Snares and the Entake Peg System (which contain these snares) are being recalled because the looped portion of the snare can become de. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The Polypectomy Snares and the Entake Peg System (which contain these snares) are being recalled because the looped portion of the snare can become detached and drop into the stomach or other internal canal during use, necessitating retrieval of the remaining piece.
Recommended Action
Per FDA guidance
Bard contacted all 1,883 worldwide customers who received the distributed suspect 467 product code lots, comprising 177, 614 units that were either not expired or were still available in the field. These will be returned by the customer to Bard Access Systems. 1-800-290-1689.
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