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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 7 of 7 Results
510(K) Number: K904440
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Product Description
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FDA Recall
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I-Flow ON-Q Pain Relief System, T-Block Needle/Catheter Tray, Model #TBTB1089T The intended use o... 2 06/03/2013 I-Flow LLC
I-Flow ON-Q Pain Relief System, T-Block Needle/Catheter Kit, Model #TB089T The intended use of ea... 2 06/03/2013 I-Flow LLC
Kimberly Clark * Nerve Root Block Tray * Single Use * Sterile * Rx only * Manufactured by Ballard Me... 2 05/16/2006 Kimberly-Clark Corporation
Kimberly Clark * Universal Block Tray * Single Use * Sterile * Rx only * Manufactured by Ballard Med... 2 05/16/2006 Kimberly-Clark Corporation
Kimberly Clark * Nerve Block Tray * Single Use * Sterile * Rx only * Manufactured by Ballard Medical... 2 05/16/2006 Kimberly-Clark Corporation
Kimberly Clark * Facet Block Tray * Single Use * Sterile * Rx only * Manufactured by Ballard Medical... 2 05/16/2006 Kimberly-Clark Corporation
Kimberly Clark * Selective Nerve Block Tray * Single Use * Sterile * Rx only * Manufactured by Balla... 2 05/16/2006 Kimberly-Clark Corporation
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