Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
The pump (with cushioning foam inserts) is packaged in a Recalled by WalkMed Infusion, LLC Due to WalkMed Infusion, LLC Announces a Voluntary Field Action...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact WalkMed Infusion, LLC directly.
Affected Products
The pump (with cushioning foam inserts) is packaged in a single pump box. Four pump boxes are placed in an over-shipper for distribution.
Quantity: 2482 units
Why Was This Recalled?
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).
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About WalkMed Infusion, LLC
WalkMed Infusion, LLC has 19 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report