PlainRecalls
FDA Devices Moderate Class II Terminated

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 body fluids, using photometric, turbidimetric, chemiluminescent, and integrated ion selective electrode technology for clinical use. Humidity packs maintain reagent compartment humidity between 70100%. The operator loads 7 empty humidity packs initially.

Reported: March 11, 2020 Initiated: January 6, 2020 #Z-1435-2020

Product Description

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 body fluids, using photometric, turbidimetric, chemiluminescent, and integrated ion selective electrode technology for clinical use. Humidity packs maintain reagent compartment humidity between 70100%. The operator loads 7 empty humidity packs initially.

Reason for Recall

A software error is causing the analyzer to incorrectly eject affected Humidity Packs as expired.

Details

Units Affected
2149
Distribution
Domestic distribution nationwide. Foreign distribution worldwide.
Location
Tarrytown, NY

Frequently Asked Questions

What product was recalled? ▼
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 body fluids, using photometric, turbidimetric, chemiluminescent, and integrated ion selective electrode technology for clinical use. Humidity packs maintain reagent compartment humidity between 70100%. The operator loads 7 empty humidity packs initially.. Recalled by Siemens Healthcare Diagnostics, Inc.. Units affected: 2149.
Why was this product recalled? ▼
A software error is causing the analyzer to incorrectly eject affected Humidity Packs as expired.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on March 11, 2020. Severity: Moderate. Recall number: Z-1435-2020.

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