Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K850964 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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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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