Baxter SIGMA Spectrum Infusion Pump with Master Drug Library (Version 6) (GTIN 00085412091570); Model Numbers: 35700BAX and 35700ABB. Intended to be used for the controlled administration of fluids.
FDA Recall Z-0971-2018 · Posted None
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Recalling FirmBaxter Healthcare Corporation
Recall StatusTerminated
Product CodeFRN
Date Initiated2017-10-06
Date Terminated2019-04-11
Product Quantity173,375
Reason for Recall
Certain infusion pumps may exhibit excessive wear of the pumping mechanism caused by a lack of lubrication, this could affect the occlusion of the tubing and result in over- or under-infusion.
Firm Action
An Urgent Medical Device Correction, dated October 6, 2017, was sent to customers. The letter described the problem, identified the affected device, discussed the hazard involved, and action to be taken. Customers were asked to locate the affected products at their facility. Customers should continue to follow the instructions in document 41394 Rev. A, PREVENTIVE MAINTENANCE, for their entire fleet of pumps. Baxter will inspect affected pumps. To arrange for return of devices that have failed the flow rate accuracy test, contact Baxter Healthcare Medina. If you are a dealer, wholesaler, or distributor/reseller that distributed any product to other facilities, please notify your customers of this Urgent Medical Device Correction. If there are additional questions, customers can contact their Baxter Sales Rep or Baxter Healthcare Medina at 800-356-3454.
Root Cause
Nonconforming Material/Component
Distribution Pattern
Worldwide Distribution - US, including the District of Columbia, Puerto Rico, and Canada.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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