Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K820227 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Portex Unit Dose 5 ml Normal Saline (0.9%)®®®® ® | 1 | 02/04/2019 | Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company |
| Portex 5ml Normal Saline (0.9%) Unit Dose®®®® ® | 1 | 02/04/2019 | Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company |
| Portex Unit Dose 15 ml Normal Saline ® | 1 | 02/04/2019 | Medex Cardio-Pulmonary Inc., d.b.a. Smiths Medical Company |
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