medical Class II Updated 2020-12-09

CME America, LLC recalls CME America T-Syringe Pump - NeoThrive - Product Usage: infu

Recalled Product

CME America T-Syringe Pump - NeoThrive - 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).


Hazard / Issue

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.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Model NeoThrive - Part Number(s) 100-101PSL UDI Code: Retired prior to UDI
View official government recall

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