FDAJune 14, 2016device

The pump (with cushioning foam inserts) is packaged in a single pump box. Four pump boxes are placed in an over-shipper for distribution.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

WalkMed Infusion, LLC Announces a Voluntary Field Action of the Triton Infusion Pump (model 300000) and Triton FP Infusion Pump (model 400000) Due to Unapproved Changes to the Software and Specifications of the Triton Infusion Pump (model 300000) and Unapproved Changes to the Intended Use of the Triton FP Infusion Pump (model 400000).

What to do

FDA enforcement status: Terminated

Brands named

walkmed infusionwalkmed

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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