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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 2 of 2 Results
Related Medical Device Recalls Recall Date to: 05/29/2015
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Product Description
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FDA Recall
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Z-2391-2010 - Hospira brand Symbiq Two-Channel Infuser, LIST No. 16027 Symbiq Two-Channel Infuser, List Number Configurations: 16027-04-01/03/04, 51/52, 53/54, 79/80,81/82,83/84,87/88 and 89/90 16026-27-89/90,... 2 09/09/2010 Hospira Inc
Z-2390-2010 - Hospira brand Symbiq One-Channel Infuser LIST No. 16026 Symbiq One-Channel Infuser, List Number Configurations: 16026-04-01/03/04,51/52, 53/54, 79/80, 81/82, 83/84, 87/88 and 89/90, 16026-13-25/2... 2 09/09/2010 Hospira Inc
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