C R Bard Inc Bard * Button Device Continuous Feeding Tube with 90 degree Adaptor, 18F, NON STERILE, REF 000256, Bard Access Systems, Inc., Salt Lake City, UT 84116 USA. The device is designed for use with the BARD Button Replacement Gastrostomy Device and used for enteral feeding in patients requiring long-term nutritional support. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Bard * Button Device Continuous Feeding Tube with 90 degree Adaptor, 18F, NON STERILE, REF 000256, Bard Access Systems, Inc., Salt Lake City, UT 84116 USA. The device is designed for use with the BARD Button Replacement Gastrostomy Device and used for enteral feeding in patients requiring long-term nutritional support.
Brand
C R Bard Inc
Lot Codes / Batch Numbers
Lot Numbers: HUSA1412, HUSD0045, HUSD0046, HUSD0047, HUSD0048, HUSD0049, HUSD0050, HUSD0052 and HUSD0351.
Products Sold
Lot Numbers: HUSA1412 , HUSD0045, HUSD0046, HUSD0047, HUSD0048, HUSD0049, HUSD0050, HUSD0052 and HUSD0351.
C R Bard Inc is recalling Bard * Button Device Continuous Feeding Tube with 90 degree Adaptor, 18F, NON STERILE, REF 000256, due to Possible restriction/occlusion in adaptors/tube accessories causing difficulty to infuse during routine feeding treatment.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Possible restriction/occlusion in adaptors/tube accessories causing difficulty to infuse during routine feeding treatment.
Recommended Action
Per FDA guidance
Customers were notified by letter and instructed to not use or further distribute any of the affected lot numbers. Customers were further instructed to return the recalled products to Bard Access Systems (BAS) through a return goods authorization number. Questions and requests for assistance should be directed to BAS Customer Service at 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