Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
CME America T-Syringe Pump - Ameritus 1st Enteral Pump - Recalled by CME America, LLC Due to Multiple reasons: 1) Due to wear and tear...
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 CME America, LLC directly.
Affected Products
CME America T-Syringe Pump - Ameritus 1st Enteral Pump - Product Usage: infusion of medications or fluids requiring continuous or intermittent delivery at precisely-controlled infusion rates through clinically acceptable routes of administration, including intravenous, subcutaneous, percutaneous, intra-arterial, epidural, in close proximity to nerves, and into an intra-operative site (soft tissue/body cavity/surgical wound site).
Quantity: Total pumps = 4,182 (all models)
Why Was This Recalled?
Multiple reasons: 1) Due to wear and tear of pump motor block mechanism - may cause under infusion situations without the pump alarm being generated. 2) Due to cracks, pump hardware may be damaged by fluid used during the cleaning process.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About CME America, LLC
CME America, LLC has 47 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report