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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K052221
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Product Description
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Recall
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FDA Recall
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ambIT Ambulatory Infusion Pump Cassette; Filterless, Spike, Sterile, Vol. 2.3ml, REF 220139, Sorenso... 2 11/16/2006 Sorenson Medical, Inc.
ambIT Ambulatory Infusion Pump Cassette; Filterless, Male, Sterile, Vol. 2.3ml, REF 220267, Sorenson... 2 11/16/2006 Sorenson Medical, Inc.
ambIT Ambulatory Infusion Pump Cassette; Filter, Spike, Sterile, Vol. 2.3ml, REF 220140, Sorenson Me... 2 11/16/2006 Sorenson Medical, Inc.
ambIT Ambulatory Infusion Pump Cassette; Filter, Male, Sterile, Vol. 2.3ml, REF 220266, Sorenson Med... 2 11/16/2006 Sorenson Medical, Inc.
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