Bard Access Systems, Inc 20F Tri-Funnel Replacement Gastrostomy Tube Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
20F Tri-Funnel Replacement Gastrostomy Tube
Brand
Bard Access Systems, Inc
Lot Codes / Batch Numbers
Product Code 000720. Lot number: NGPL2270.
Products Sold
Product Code 000720. Lot number: NGPL2270.
Bard Access Systems, Inc is recalling 20F Tri-Funnel Replacement Gastrostomy Tube due to Packaging for some gastrostomy tubes was labeled with incorrect balloon inflation data. An underinflated balloon may cause misplacement, slippage or p. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Packaging for some gastrostomy tubes was labeled with incorrect balloon inflation data. An underinflated balloon may cause misplacement, slippage or premature removal of the tube. If an underinflated balloon allows the tube to be placed, or slip into, the stomal tract and not the stomach, there is a risk of infusion of fluids into the peritoneum. This carries the risk of infection.
Recommended Action
Per FDA guidance
Consignees were notified by letter on 04/06/2006.
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