ClearanceBrief
Recall Z-2190-2009 ยท KNT Tubes, Gastrointestinal (And Accessories)

C.R. Bard Access Systems, Inc

Bard Access Systems, Inc., Fastrac* Guidewire Gastric Access Port Safety System, REF 007030, 24F, Sterile.

DateSep 15, 2009 (initiated Dec 4, 2008)
StatusTerminated
ReasonSnare can detach in patient. 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.
Root causeNonconforming Material/Component
ActionBard 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.
Quantity177,614 units
DistributionWorldwide, including USA, Belgium, Canada, Australia, and Japan.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K033562FASTRAC GASTRIC ACCESS PORT KIT
C.R. Bard, Inc., Dec 12, 2003
K061021ENTAKE STANDARD AND SAFETY PEG SYSTEM
Conmedcorp, Apr 28, 2006
K915841BARD GAUDERER UNIVERSAL PERCUTANEOUS ENDOSCOPIC
C.R. Bard, Inc., Jun 25, 1993
K972025RADIUS PULL PERCUTANEOUS ENDOSCOPIC GASTROSTOMY KIT
Radius Intl., Inc., Jan 23, 1998
K972101SOLITAIRE
Heraeus Kulzer, Inc., Sep 29, 1997