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U.S. Department of Health and Human Services

Medical Device Recalls
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Related Medical Device Recalls
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Z-1763-2017 - Cobas 8100 bi-directional reformatter (BRF) module with Software Version 02-xx 2 03/23/2017 Roche Diagnostics Corporation
Z-1764-2017 - Cobas 8100 uni-directional reformatter (BRF) module with Software Version 02-xx 2 03/23/2017 Roche Diagnostics Corporation
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