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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 5 of 5 Results
510(K) Number: K850964
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Product Description
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Recall
Class
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FDA Recall
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Hudson RICA® Sher-I-Swiv & Sher-I-Swiv F/O, Teleflex Medical, Research Triangle Park, NC 27709. I... 2 09/16/2009 Teleflex Medical
Hudson RICA® Sheridan, ET Tube, Sher-I-Bronch LS, 28FR, 35FR, 37FR, 39FR and 41FR, Teleflex Medical,... 2 09/16/2009 Teleflex Medical
Hudson RICA® Sheridan, EB Tube, Sher-I-Bronch, LS, 35FR, Nova Plus, 37FR, 39 FR, and 41 FR, Teleflex... 2 09/16/2009 Teleflex Medical
Hudson RICA® Sheridan, Sher-I-Bronch Accessory Pack, Teleflex Medical, Research Triangle Park, NC 27... 2 09/16/2009 Teleflex Medical
Hudson RICA® Sheridan, ET Tube, Sher-I-Bronch RS, 28FR, 35 FR, 37 FR, 39FR and 41 FR, Teleflex Medic... 2 09/16/2009 Teleflex Medical
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