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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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Product Description
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FDA Recall
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Z-1436-2020 - Atellica IM Humidity Pack (Qty 1), SMN 11313496, UDI 00630414243726, Software Version V1.21.0 and lower - Product Usage: Product Usage: The system is intended for the qualitative and quantitative anal... 2 03/04/2020 FEI # 2432235
Siemens Healthcare Diagnostics, Inc.
Z-1435-2020 - Atellica IM Humidity Pack (Qty 5), SMN 11313505, UDI 00630414234526, Software Version V1.21.0 and lower - Product Usage: The system is intended for the qualitative and quantitative analysis of various... 2 03/04/2020 FEI # 2432235
Siemens Healthcare Diagnostics, Inc.
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