Medical Device Recalls
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21 to 25 of 25 Results
510(K) Number: K051641 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
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Alaris PC unit model 8015 Product Usage: The device is labeled for prescription use only. | 1 | 07/26/2012 | CareFusion 303, Inc. |
Alaris PC unit model 8000 and 8015 with Alaris PCA module model 8120 and Auto ID barcode scanner mod... | 1 | 12/20/2013 | CareFusion 303, Inc. |
Alaris PC unit Model 8000 only when used with Alaris Pump module or Alaris Syringe module | 2 | 06/26/2015 | CareFusion Corporation |
Alaris PC Unit, Model 8015 | 2 | 06/19/2017 | CareFusion 303, Inc. |
Alaris PC Unit, Infusion Pump Model 8000, Part No. TC10005092 | 2 | 03/24/2016 | CareFusion 303, Inc. |
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