CME America recalls NeoThrive T-Syr: pumps may under-infuse medications without alarm due to motor wear or cracks. Affected models include 100-101PSL. Stop using immediately to prevent medication errors.
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.
CME America recalls its NeoThrive T-Syringe Pump for possible under-infusion of medications without alarms. This could lead to incorrect medication dosing if the pump fails during use.
The pump's motor mechanism may wear out, causing it to under-infuse medications without triggering the alarm. Cracks in the pump hardware could also be damaged by cleaning fluids, leading to potential failure during use.
People using the NeoThrive pump for medical infusions, especially those with chronic conditions requiring precise medication delivery. Those who rely on the pump for continuous or intermittent fluid administration are most at risk.
Check for the model number 100-101PSL on the pump. The NeoThrive pump is used for continuous or intermittent medication infusions through clinical routes like IV or subcutaneous delivery.
The pump may under-infuse medications without alarms, risking incorrect dosing. Do not continue using the device.
No, the pump may under-infuse medications without alarms due to motor wear or cracks, so it should not be used.
The affected model is 100-101PSL.
Check for the model number 100-101PSL on the pump, which is used for continuous or intermittent medication infusions.
We’ve drafted a message you can send CME America to request your refund or repair — edit it as you like.
Subject: Recall Z-0526-2021 — CME America CME America Hello, I own a CME America that is covered by recall Z-0526-2021 from CME America. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
