Skip to content
Recall Observatory FDA recall evidence

Device product

Baxter SIGMA Spectrum INFUSION PUMP with Master Drug Library, V8 Spectrum Infusion Pump, Product Code 35700BAX2, Unique Device Identifier GTIN 00085412091570, Rx ONLY -- Baxter Healthcare Corporation, Medina, NY 14103 --- NOTE: The speakers are a part of the rear case assembly located in the back of the infusion pump. The speaker is intended to generate audible tones during each keystroke, and during alarm conditions. However, some speakers have a variation in their internal wiring that increases the potential for the speaker to fail prematurely. Spectrum Infusion Pumps with non-functional speakers will continue to display visual alarm indications, and will otherwise continue to operate as intended.

Z-0671-2017

September 28, 2016

Class II

Product summary

Firm
Baxter Healthcare Corp.
Event
Event 75311
Status
Terminated
Classification
Class II
Quantity
15,517 units (US: 9560; Canada: 5957)
Official record key
device-enforcement:Z-0671-2017

Official wording

Reason: A correction was issued for the SIGMA Spectrum Infusion Pump with Master Drug Library in order to replace speakers installed in pumps or included in spare part rear case assemblies that have an increased potential to fail prematurely.

Code information: Contact CDRH for list of affected serial numbers (15,517).

Distribution pattern: Nationwide Distribution, Puerto Rico and Canada

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    A correction was issued for the SIGMA Spectrum Infusion Pump with Master Drug Library in order to replace speakers installed in pumps or included in spare part rear case assemblies that have an increased potential to fail prematurely.