Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K982159 |
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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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| The Plum A+ Infusion System is a cassette based multifunction infusion system that allows two lines ... | 2 | 11/14/2013 |
FEI # 3013319212 Hospira Inc. |
| Plum A+ Infusion Pump; List Number: 11973; Product Usage: The Plum A+ Infusion Systems are ... | 2 | 11/14/2013 |
FEI # 3013319212 Hospira Inc. |
| LifeShield LATEX-FREE HemoSet 100 mL Burette I.V. PlumSet, Nonvented, 105 inch with Prepierced Resea... | 2 | 04/21/2014 |
FEI # 3013319212 Hospira Inc. |
| *** 1) Product labeled in part: 19683-28; LIFESHIELD; MICRODRIP SOLUSET WITH 1.2 MICRON FILTER 150ML... | 2 | 06/29/2016 |
FEI # 3013319212 Hospira Inc. |
| *** 1) Product labeled in part: 14951-48; LIFESHIELD; PLUMSET WITH CONVERTIBLE PIERCING PIN, TWO INT... | 2 | 06/29/2016 |
FEI # 3013319212 Hospira Inc. |
| Infusion Pump I.V. Administration, specifically Plum Microbore Infusion Sets with Inline Filters lab... | 2 | 10/14/2019 |
FEI # 3013319212 ICU Medical Inc |
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