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Sigma Spectrum Infusion Pumps with Master Drug Library by Baxter Healthcare: Recall

Includes Model No. 35700BAX and 35700ABB

Baxter has received over 3,500 reports of System Error 322 Link Switch Error (low) incidents in which the device has malfunctioned, including nine severe adverse events and no deaths. The System Error 322 occurs when the pump improperly detects that the door is open when it is physically closed. A System Error 322 may lead to an interruption or delay in therapy.

If the System 322 occurs, the Sigma Spectrum Infusion Pump stops the infusion, an alarm sounds, and a light flashes (a visual 322 alarm). This requires a clinician to reset the alarm, reprogram the pump, and confirm the infusion is running properly.

The use of affected product may cause serious adverse health consequences, including death.

If you or a loved one has been injured as a result of a Sigma Spectrum Infusion Pumps malfunction or any other drug or medical device, including Stryker Rejuvinate and ABG II Hip Implants, Zimmer, Nex Gen Knee Implants, Post-Operative Disposable Pain Pumps, or GranuFlo and NaturalLyte Dialysis Products, the law office of Hicks & Motto can help. Since 1987 Hicks & Motto have been representing the injured victims of negligence and defective products.

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