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U.S. Department of Health and Human Services

Medical Device Recalls

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11 to 20 of 29 Results
510(K) Number: K033562
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Product Description
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FDA Recall
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Bard Access Systems, Inc., Fastrac* Guidewire Gastric Access Port Safety System, REF 007024, 20F, St... 2 09/15/2009 C.R. Bard Access Systems, Inc
Bard Access Systems, Inc., Fastrac* Guidewire Gastric Access Port Safety System, REF 007030, 24F, St... 2 09/15/2009 C.R. Bard Access Systems, Inc
Bard Access Systems, Inc., Fastrac* Guidewire Gastric Access Port Safety System, REF 007035, 24F, St... 2 09/15/2009 C.R. Bard Access Systems, Inc
Bard Access Systems, Inc., Fastrac* "Pull" Gastric Access Port Kit, REF 007036, 24F, Sterile. 2 09/15/2009 C.R. Bard Access Systems, Inc
Bard Access Systems, Inc., Fastrac* "Pull" Gastric Access Port Kit, REF 007037, 16F, Sterile. 2 09/15/2009 C.R. Bard Access Systems, Inc
Bard Access Systems, Inc., Fastrac* "Pull" Gastric Access Port Kit, REF 007038, 14F, Sterile. 2 09/15/2009 C.R. Bard Access Systems, Inc
Bard Access Systems, Inc., Fastrac* "Pull" Gastric Access Port Kit, REF 007050, 24F, Sterile. 2 09/15/2009 C.R. Bard Access Systems, Inc
Bard Access Systems, Inc., Fastrac* "Pull" Gastric Access Port Safety System, REF 007052, 16F, Steri... 2 09/15/2009 C.R. Bard Access Systems, Inc
Bard Access Systems, Inc., Fastrac* "Pull" Gastric Access Port Safety System, REF 007056, 14F, Steri... 2 09/15/2009 C.R. Bard Access Systems, Inc
Bard Access Systems, Inc., Fastrac* "Pull" Gastric Access Port Kit, REF 007078, 20F, Sterile. 2 09/15/2009 C.R. Bard Access Systems, Inc
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