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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
Related Medical Device Recalls
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Product Description
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Class
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FDA Recall
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Z-1940-2009 - Hudson RICA® Sher-I-Swiv & Sher-I-Swiv F/O, Teleflex Medical, Research Triangle Park, NC 27709. Indicated for use in thoracic surgery, bronchospirometry, for the administration of endobronchial ane... 2 09/16/2009 Teleflex Medical
Z-1941-2009 - Hudson RICA® Sheridan, ET Tube, Sher-I-Bronch LS, 28FR, 35FR, 37FR, 39FR and 41FR, Teleflex Medical, Research Triangle Park, NC 27709. Indicated for use in thoracic surgery, bronchospirometry, for ... 2 09/16/2009 Teleflex Medical
Z-1944-2009 - Hudson RICA® Sheridan, EB Tube, Sher-I-Bronch, LS, 35FR, Nova Plus, 37FR, 39 FR, and 41 FR, Teleflex Medical, Research Triangle Park, NC 27709. Indicated for use in thoracic surgery, bronchospirome... 2 09/16/2009 Teleflex Medical
Z-1943-2009 - Hudson RICA® Sheridan, Sher-I-Bronch Accessory Pack, Teleflex Medical, Research Triangle Park, NC 27709. Indicated for use in thoracic surgery, bronchospirometry, for the administration of endobron... 2 09/16/2009 Teleflex Medical
Z-1942-2009 - Hudson RICA® Sheridan, ET Tube, Sher-I-Bronch RS, 28FR, 35 FR, 37 FR, 39FR and 41 FR, Teleflex Medical, Research Triangle Park, NC 27709. Indicated for use in thoracic surgery, bronchospirometry, f... 2 09/16/2009 Teleflex Medical
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