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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K910492
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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18F Tri-Funnel Replacement Gastrostomy Tube 2 05/03/2006 Bard Access Systems, Inc
24F Tri-Funnel Replacement Gastrostomy Tube 2 05/03/2006 Bard Access Systems, Inc
22F Tri-Funnel Replacement Gastrostomy Tube 2 05/03/2006 Bard Access Systems, Inc
20F Tri-Funnel Replacement Gastrostomy Tube 2 05/03/2006 Bard Access Systems, Inc
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