Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K960857 |
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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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LH Lithium Heparin tubes, Greiner bio-one, North America, 4238 Capital Drive, Monroe, NC 28110. V... | 2 | 02/22/2012 | Greiner Bio-One North America, Inc. |
VACUETTE®, 2 ml Lithium Heparin Venous Blood Collection Tubes. Reference #454237, 13x75 green cap-w... | 3 | 11/07/2008 | Greiner Bio-One North America, Inc. |
Vacuette 2 ml Lithium Heparin, Collection Tube, Manufactured by: Greiner-Bio One North America, Inc.... | 2 | 12/16/2010 | Greiner Bio-One North America, Inc. |
greiner bio-one VACUETTE TUBE, 5 ml LH Lithium Heparin Sep, 13x100 green cap-yellow ring, non-ridged... | 2 | 01/18/2022 | Greiner Bio-One North America, Inc. |
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