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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K942329
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Product Description
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Recall
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FDA Recall
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Angiographic Syringe, 10 cc Thumb Ring with Rotator Reservoir. 2 03/15/2005 FEI # 3013319212
Hospira Inc.
Angiographic Syringe, 12 cc Palm Pad with Rotator Reservoir. 2 03/15/2005 FEI # 3013319212
Hospira Inc.
Angiographic Syringe, 12 cc Thumb Ring with Rotator Non-Reservoir. 2 03/15/2005 FEI # 3013319212
Hospira Inc.
Angiographic Syringe, 12 cc Thumb Ring with Rotator Reservoir. 2 03/15/2005 FEI # 3013319212
Hospira Inc.
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