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U.S. Department of Health and Human Services

Medical Device Recalls
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11 to 14 of 14 Results
510(K) Number: K031560
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Product Description
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FDA Recall
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Brand Name: RapidLab 1200 System, Model 1260, Part Number 05062460; All RapidLab 1200 Systems with ... 2 03/29/2006 Bayer Healthcare, LLC (Diagnostics Division)
Brand Name: RapidLab 1200 System, Model 1245, Part Number 05061537; All RapidLab 1200 Systems with S... 2 03/29/2006 Bayer Healthcare, LLC (Diagnostics Division)
Brand Name: RapidLab 1200 System, Model 1240, Part Number 05060298; All RapidLab 1200 Systems with S... 2 03/29/2006 Bayer Healthcare, LLC (Diagnostics Division)
Brand Name: RapidLab 1200 System, Model 1265, Part Number 05063769; All RapidLab 1200 Systems with ... 2 03/29/2006 Bayer Healthcare, LLC (Diagnostics Division)
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