CME America, LLC: Medical Device Recall in 2020 - (Recall #: Z-0526-2021)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

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).

Product Classification:

Class II

Date Initiated: July 30, 2020

Date Posted: December 9, 2020

Recall Number: Z-0526-2021

Event ID: 86047

Reason for Recall:

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.

Status: Terminated

Product Quantity: Total pumps = 4,182 (all models)

Code Information:

Model NeoThrive - Part Number(s) 100-101PSL UDI Code: Retired prior to UDI

Distribution Pattern:

Worldwide distribution - U.S. Nationwide distribution including in the states of AZ, AK, CA, CO, CT, FL, ID, IL, KS, LA, MA, MI, MO, MT, NC, NE, NV, Oh, OK, OR, PA, TN, TX, WA, and WI. The country of Canada.

Voluntary or Mandated:

Voluntary: Firm initiated