C R Bard Inc Dual Port Wizard Low Profile Replacement Gastrostomy Device, REF 00200W, 16F x 1.2cm, 10cc, Sterile EO, Bard Access Systems, Inc., Salt Lake City, UT 84116. A silicone low-profile balloon-type device is designed for percutaneous insertion through an established, appropriately sized stoma tract. It is a component of the Dual Port Wizard Gastrostomy Device. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Dual Port Wizard Low Profile Replacement Gastrostomy Device, REF 00200W, 16F x 1.2cm, 10cc, Sterile EO, Bard Access Systems, Inc., Salt Lake City, UT 84116. A silicone low-profile balloon-type device is designed for percutaneous insertion through an established, appropriately sized stoma tract. It is a component of the Dual Port Wizard Gastrostomy Device.
Brand
C R Bard Inc
Lot Codes / Batch Numbers
Lot numbers: HUSC0041, HUSC0042, HUSD0281, HUSD0326, HUSD1983, HUSD1984, HUSE1554, HUSF1907, HUSF1908, HUSG1086, HUSG1087, HUSH1621, HUSH1651, HUSI2748 and HUSI2749.
Products Sold
Lot numbers: HUSC0041, HUSC0042, HUSD0281, HUSD0326, HUSD1983, HUSD1984, HUSE1554, HUSF1907, HUSF1908, HUSG1086, HUSG1087, HUSH1621, HUSH1651, HUSI2748 and HUSI2749.
C R Bard Inc is recalling Dual Port Wizard Low Profile Replacement Gastrostomy Device, REF 00200W, 16F x 1.2cm, 10cc, Sterile due to Out of specification replacement gastrostomy device was distributed.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Out of specification replacement gastrostomy device was distributed.
Recommended Action
Per FDA guidance
Consignees were notified by "Product Recall" letter distributed on January 7, 2009 via Federal Express overnight mail and asked to check all inventory locations, remove unused affected product and return to Bard Access Systems, Inc (BAS). Customers were also instructed to complete the enclosed Reply Form and Inventory Reconciliation Form and fax it to BAS at 1-801-522-5674. Additional information is available by calling BAS Customer Service at 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 noticeDistribution
As reported by FDA
AL, AZ, CA, CO, CT, FL, GA, IL, IA, KS, KY, LA, ME, MD, MA, MI, MN, MS, MO, NE, NH, NJ, NM, NY, NC, ND, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WV, WI
Page updated: Jan 10, 2026