Medical Device Recalls
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11 to 16 of 16 Results
510(K) Number: K932188 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Bifurcated SafeSet Kit with 03mL Flush Device, Item No. 46091-75 Product Usage: The Transpac D... | 2 | 09/15/2016 | ICU Medical, Inc. |
Pediatric Kit with 30mL Flush Device, Item No. 46099-10 Product Usage: The Transpac Disposable... | 2 | 09/15/2016 | ICU Medical, Inc. |
Angiographic Syringe, 12 cc Palm Pad with Rotator Reservoir. | 2 | 03/15/2005 | Hospira Inc. |
Angiographic Syringe, 12 cc Thumb Ring with Rotator Non-Reservoir. | 2 | 03/15/2005 | Hospira Inc. |
Angiographic Syringe, 12 cc Thumb Ring with Rotator Reservoir. | 2 | 03/15/2005 | Hospira Inc. |
Angiographic Syringe, 10 cc Thumb Ring with Rotator Reservoir. | 2 | 03/15/2005 | Hospira Inc. |
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