Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K123874 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| ***Baxter***Buretrol Solution Set***105" (2.7 m)***150 mL Burette***Drip Chamber Filter Valve***3 In... | 2 | 09/09/2014 | Baxter Healthcare Corp |
| ***Baxter***Non-DEHP***BURETROL Solution Set 105" (2.7 m), 150 mL Burette***Drip Chamber Filter Val... | 2 | 09/09/2014 | Baxter Healthcare Corp |
| ***Baxter***BURETROL Solution Set***105" (2.7 m) 150 mL Burette***Drip Chamber Filter Valve***3 Lue... | 2 | 09/09/2014 | Baxter Healthcare Corp |
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