Medical Device Recalls
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21 to 26 of 26 Results
510(K) Number: K032438 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Tyco HealthcareMonoject Prefill 10U/mL Heparin Lock Flush Syringe, 3mL REF # 8881580123, Tyco Heal... | 2 | 05/09/2008 |
FEI # 1282497 Covidien LP |
| Tyco Healthcare Tyco HealthcareMonoject Prefill 10U/mL Heparin Lock Flush Syringe 5mL REF # 888158... | 2 | 05/09/2008 |
FEI # 1282497 Covidien LP |
| Monoject 0.9% Sodium Chloride, Flush Prefilled Syringe, 10 mL, REF: 8881570121 inside the following ... | 1 | 10/29/2021 |
FEI # 1000125955 Windstone Medical Packaging, Inc. |
| Monoject 0.9% Sodium Chloride Flush Syringe, 10 mL Fill, STERILE, Product Code 8881570121 The pr... | 1 | 08/21/2021 |
FEI # 3014524790 Cardinal Health |
| Monoject 0.9% Sodium Chloride Flush Syringe, 3 mL Fill, STERILE, Product Code 8881570123 The pro... | 1 | 08/21/2021 |
FEI # 3014524790 Cardinal Health |
| Monoject 0.9% Sodium Chloride Flush Syringe, 5mL Fill, STERILE, Product Code 8881570125 The prop... | 1 | 08/21/2021 |
FEI # 3014524790 Cardinal Health |
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