Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K943803 |
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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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| Maquet HL Console for Heart Lung Machine HL20 HL 20 4-pumps console base: P/N 917741 HL 20 5-pumps... | 2 | 08/29/2011 |
FEI # 3008355164 Maquet Inc. |
| Maquet HL Console for Heart Lung Machine HL20: HL 20 4-pumps console base: P/N 917741 HL 20 5-pump... | 2 | 08/22/2011 |
FEI # 3008355164 Maquet Inc. |
| Maquet Cardiopulmonary AG, MAQUET RPM 20: Roller Pump for Heart Lung Machine HL20. | 2 | 02/22/2011 |
FEI # 3008355164 Maquet Cardiovascular Us Sales, Llc |
| Jostra - HL-20 Heart Lung Integrated Perfusion System, Roller Pump Hand crank | 2 | 11/07/2006 |
FEI # 3008355164 MAQUET Inc. |
| Jostra HL-20 Heart Lung Machine - guiding pins | 2 | 11/07/2006 |
FEI # 3008355164 MAQUET Inc. |
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