Medical Device Recalls
-
1 to 2 of 2 Results
510(K) Number: K971239 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
VACUETTE TUBE 4 ml FX Sodium Fluoride/Potassium Oxalate, Item #454297, 13x75 grey cap-black ring, no... | 2 | 01/16/2024 | Greiner Bio-One North America, Inc. |
4 ml FX Sodium Fluoride/Potassium Oxalate tube, Ref 454297 VACUETTE Glycolytic Inhibitor Tubes cont... | 2 | 06/07/2016 | Greiner Bio-One North America, Inc. |
-