Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K952799 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Plum XL3M, List numbers 11845-04-03, 11845-04-05, 11845-04-07, 11845-04-11, 11845-04-13; AC cord man... | 2 | 10/06/2009 | Hospira Inc |
| Plum XLM, list #s 11846-04-03, 11846-04-05, 11846-04-07; AC cord manufactured by Electri-Cord, Westf... | 2 | 10/06/2009 | Hospira Inc |
| Hospira Plum XL Micro/Macro Infusion Pump, Single Channel, with a 0.1-999 mL/hr flow rate range; li... | 2 | 03/08/2011 | Hospira Inc. |
| Hospira Plum XL3 Micro/Macro Infusion Pump, Triple Channel, with a 0.1-999 mL/hr flow rate range; ... | 2 | 03/08/2011 | Hospira Inc. |
| Hospira Plum XL3 Micro/Macro with DataPort Infusion Pump, Triple Channel, with a 0.1-999 mL/hr flow ... | 2 | 03/08/2011 | Hospira Inc. |
| Plum XL3 Multi line Infusion System, Micro Macro Plum XL3 Multi line Infusion System, and Micro Macr... | 2 | 06/03/2014 | Hospira Inc. |
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