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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: K954340
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Product Description
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Recall
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FDA Recall
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Bausch & Lomb MicroFlow 45® Phaco Needle, Model DP8245S, 6 pouches/box. The firm name on the label ... 2 05/28/2010 Bausch & Lomb Inc
Bausch & Lomb MicroFlow 30® Phaco Needle, Model DP8230S, 6 pouches/box. The firm name on the label ... 2 05/28/2010 Bausch & Lomb Inc
Bausch & Lomb MicroFlow 2.2 30® Phaco Needle, Model DP8730S, 6 pouches/box. The firm name on the l... 2 05/28/2010 Bausch & Lomb Inc
Bausch & Lomb MicroFlow Plus 30® Phaco Needle, Model DP8330S, 6 pouches/box. The firm name on the l... 2 05/28/2010 Bausch & Lomb Inc
Microflow Needles, catalog #DP8200, with 0 degree tapering, labeled in part ***Non-sterile, Manufact... 2 10/15/2003 Bausch & Lomb Incorporated
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