CME America recalls Ameritus 1st Enteral Pump due to potential under infusion without alarm. Check serial numbers listed to see if your pump is affected.
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 is recalling its Ameritus 1st Enteral Pump because it may cause under infusion without triggering the pump alarm. This could lead to improper medication delivery if the pump fails to alert the user.
The pump's motor block mechanism can wear out, causing under infusion without the alarm sounding. Additionally, cracks in the pump hardware may be damaged during cleaning with fluids, potentially leading to malfunction.
People using this pump for medical infusions, such as those receiving medications or fluids through IV, subcutaneous, or other clinical routes. Patients with chronic conditions requiring precise fluid delivery are most at risk.
This pump has serial numbers starting with 58768-58770, 26411-26483, 26484-26485, 26486-26487, and other numbers listed in the recall notice. The product is used for medical infusions requiring precise control.
Look for the serial number on the pump's label to see if it matches the list of affected numbers provided in the recall.
The pump may cause under infusion without triggering the alarm due to wear and tear of the motor block mechanism. Cracks in the hardware can also be damaged during cleaning with fluids.
Check the pump's serial number against the list of affected numbers provided in the recall notice. If it matches, stop using it and contact CME America for further instructions.
The recall record does not specify a remedy, so no fix is provided. Affected users should check the serial number and contact the manufacturer.
We’ve drafted a message you can send CME America to request your refund or repair — edit it as you like.
Subject: Recall Z-0529-2021 — CME America CME America Hello, I own a CME America that is covered by recall Z-0529-2021 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
